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Drug Classes

2. Anti-infectives

3. Cephalosporins
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Cephalosporins
Written by C. Fookes, BPharm on Jul 20, 2018

What are Cephalosporins?


Cephalosporins are a large group of antibiotics derived from the
mold Acremonium (previously called Cephalosporium). Cephalosporins are
bactericidal (kill bacteria) and work in a similar way to penicillins. They bind to
and block the activity of enzymes responsible for making peptidoglycan, an
important component of the bacterial cell wall. They are called broad-spectrum
antibiotics because they are effective against a wide range of bacteria.

Since the first cephalosporin was discovered in 1945, scientists have been
improving the structure of cephalosporins to make them more effective against a
wider range of bacteria. Each time the structure changes, a new "generation" of
cephalosporins are made. So far there are five generations of cephalosporins. All
cephalosporins start with cef, ceph, or kef. Note that this classification system is
not used consistently from country to country.

What are cephalosporins used for?


Cephalosporins may be used to treat infections caused by susceptible bacteria,
such as:

 Bone infections
 Ear infections (eg, otitis media)
 Skin infections
 Upper respiratory tract infections
 Urinary tract infections.
Cephalosporins are not usually used as a first-choice antibiotic. They tend to be
reserved for use when other antibiotics (often penicillins) cannot be used.

What are the differences between


cephalosporins?
There are currently five “generations” of cephalosporins, with each generation
differing slightly in their antibacterial spectrum (ie, how effective they are at
killing certain types of bacteria). Within each generation, there are differences in
terms of administration (such as oral or intravenous administration), absorption,
excretion, and how long the activity of the cephalosporin lasts for in the body.

First generation cephalosporins

First generation cephalosporins refer to the first group of cephalosporins


discovered. Their optimum activity is against gram-positive bacteria such
as staphylococci and streptococci. They have little activity against gram-negative
bacteria.

Cephalexin and cefadroxil can be given by mouth, whereas cefazolin can only
be given by injection (IV/IM). There are also differences with regards to how
frequently the different first-generation cephalosporins need to be dosed.

Generic name Brand name examples

cefadroxil Duricef

cefazolin Ancef, Kefzol

cephadrine Discontinued

cephalexin Daxbia, Keflex

Second generation cephalosporins

Second-generation cephalosporins are more active against gram-negative


bacteria, with less activity against gram-positive bacteria.
Generic name Brand name examples

cefotetan Cefotan

cefoxitin Mefoxin

cefprozil Cefzil

cefuroxime Ceftin, Zinacef

loracarbef Discontinued

Third generation cephalosporins

Third generation cephalosporins followed the second-generation cephalosporins.


No one third-generation cephalosporin treats all infectious disease scenarios.

Cefotaxime and ceftizoxime (discontinued) offer the best gram-positive


coverage out of all the third-generation agents; ceftazidime and cefoperazone
(discontinued) are unique in that they provide antipseudomonal coverage.

Ceftriaxone has a long half-life which allows for once daily dosing and may be
used for the treatment of gonorrhea, pelvic inflammatory disease, and
epididymo-orchitis. It is also an alternative to penicillins for
suspected meningitis.

All the third-generation cephalosporins except for cefoperazone (discontinued)


penetrate cerebrospinal fluid.

Generic name Brand name examples

cefdinir Omnicef

cefditoren Spectracef

cefixime Suprax

cefoperazone Discontinued

cefotaxime Claforan

cefpodoxime Generic
Generic name Brand name examples

ceftazidime Fortaz, Tazicef

ceftibuten Cedax

ceftriaxone Generic

Fourth generation cephalosporins

Fourth generation cephalosporins are structurally related to third-generation


cephalosporins but possess an extra ammonium group, which allows them to
rapidly penetrate through the outer membrane of gram-negative bacteria,
enhancing their activity. They are also active against β-lactamase
producing Enterobacteriaceae which may inactivate third-generation
cephalosporins.

Some fourth-generation cephalosporins have excellent activity against gram-


positive bacteria such as methicillin-susceptible staphylococci, penicillin-
resistant pneumococci, and viridans group streptococci.

Cefepime is the only fourth generation cephalosporin available in the United


States. Cefpirome is available overseas.

Generic name Brand name examples

cefepime Maxipime

Next (fifth) generation cephalosporins

Ceftaroline is currently the only next-generation cephalosporin available in the


United States. It is active against methicillin-resistant Staphylococcus
aureus (MRSA) and gram-positive bacteria. It also retains the activity of the later-
generation cephalosporins and is effective against susceptible gram-negative
bacteria.

Generic name Brand name examples

ceftaroline Teflaro
Are cephalosporins safe?
Cephalosporins are generally safe, with low toxicity and good efficacy against
susceptible bacteria.

Allergic reactions have been reported with cephalosporins and symptoms may
include a rash, hives (urticaria), swelling, or rarely, anaphylaxis. Up to 10% of
people with a history of penicillin allergy will also be allergic to cephalosporins.

Rarely, seizures have been reported with some cephalosporins; the risk is
greatest in those with kidney disease.

Cephalosporins have also been associated with a reduced ability of the blood to
clot leading to prolonged bleeding times. People with kidney or liver disease,
nutritionally deprived, taking cephalosporins long-term, or concurrently receiving
anticoagulant therapy are more at risk.

For a complete list of severe side effects, please refer to the individual drug
monographs.

What are the side effects of cephalosporins?


Cephalosporins generally cause few side effects. The most common side effects
reported include abdominal pain, diarrhea, dyspepsia, headache, gastritis,
and nausea and vomiting. Transient liver problems have also been reported.

Rarely, some people may develop a super-infection due to overgrowth of a


naturally occurring bacterium called Clostridium difficile, following use of any
antibiotic, including cephalosporins. Symptoms may include severe diarrhea.

Uncommonly, an overgrowth of the yeast, Candida albicans, may occur following


cephalosporin use, resulting in the symptoms of thrush.
What are Cephalosporins/beta-lactamase
inhibitors?
Cephalosporins are a group of broad spectrum, semi-synthetic beta-lactam
antibiotics derived from the mould Cephalosporium. The mechanism of action of
cephalosporins is the same as penicillins in that they interfere with bacterial cell
wall synthesis. They are classified according to the chronological order in which
they were produce. Beta-lactamase inhibitors block the activity of beta-lactamase
enzymes. Some species of bacteria produce beta-lactamase enzymes, which
cleave the beta-lactam group in antibiotics, such as cephalosporins, that have a
beta-lactam ring in their structure. In doing so the beta-lactamase enzyme
inactivates the antibiotic and becomes resistant to that antibiotic. To avoid
development of resistance, beta-lactamase inhibitors are administered with the
beta-lactam antibiotics so the action of beta-lactamase is inhibited. This tends to
widen the spectrum of antibacterial activity.

List of Cephalosporins/beta-lactamase
inhibitors:
Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Avycaz (Pro) 0 reviews Add rating


Generic name: avibactam / ceftazidime

Zerbaxa (Pro)
Generic name: ceftolozane / tazobactam
1. Drug Classes

2. Anti-infectives

3. Cephalosporins
4. First Generation Cephalosporins
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First generation cephalosporins


Written by C. Fookes, BPharm on Jun 29, 2018

What are First generation cephalosporins?


Cephalosporins are a large group of antibiotics derived from the mold
Acremonium (previously called Cephalosporium). Cephalosporins are bactericidal
(kill bacteria) and work in a similar way to penicillins. They bind to and block the
activity of enzymes responsible for making peptidoglycan, an important
component of the bacterial cell wall. They are called broad-spectrum antibiotics
because they are effective against a wide range of bacteria.

Since the first cephalosporin was discovered in 1945, scientists have been
improving the structure of cephalosporins to make them more effective against a
wider range of bacteria. Each time the structure changes, a new "generation" of
cephalosporins are made. So far there are five generations of cephalosporins. All
cephalosporins start with cef, ceph, or kef. Note that this classification system is
not used consistently from country to country.

First generation cephalosporins refer to the first group of cephalosporins


discovered. Their optimum activity is against gram-positive bacteria such
as staphylococci and streptococci. They have little activity against gram-negative
bacteria.

What are first generation cephalosporins


used for?
First generation cephalosporins may be used to treat infections caused by
susceptible bacteria such as:
 Bone infections
 Ear infections (eg, otitis media)
 Skin infections
 Upper respiratory tract infections
 Urinary tract infections.

What are the differences between first


generation cephalosporins?
Cephalexin and cefadroxil can be given by mouth, whereas cefazolin can only
be given by injection (IV/IM). There are also differences with regards to how
frequently the different first-generation cephalosporins need to be dosed.

Generic name Brand name examples

cefadroxil Duricef

cefazolin Ancef, Kefzol

cephadrine Discontinued

cephalexin Daxbia, Keflex

Are first generation cephalosporins safe?


First generation cephalosporins are generally safe, with low toxicity and good
efficacy against susceptible bacteria.

Allergic reactions have been reported with cephalosporins (including first


generation cephalosporins) and symptoms may include a rash, hives (urticaria),
swelling, or rarely, anaphylaxis. Up to 10% of people with a history of penicillin
allergy will also be allergic to cephalosporins.
Rarely, seizures have been reported with some cephalosporins; the risk is
greatest in those with kidney disease.

Cephalosporins have also been associated with a reduced ability of the blood to
clot leading to prolonged bleeding times. People with kidney or liver disease,
nutritionally deprived, taking cephalosporins long-term, or concurrently receiving
anticoagulant therapy are more at risk.

For a complete list of severe side effects, please refer to the individual drug
monographs.

What are the side effects of first generation


cephalosporins?
First generation cephalosporins generally cause few side effects. The most
common side effects reported
include diarrhea, nausea and vomiting, dyspepsia, gastritis and abdominal
pain. Transient liver problems have also been reported.

Rarely, some people may develop a super-infection due to overgrowth of a


naturally occurring bacterium called Clostridium difficile, following use of any
antibiotic, including cephalosporins. Symptoms may include severe diarrhea.

Uncommonly, an overgrowth of the yeast, Candida albicans, may occur following


cephalosporin use, resulting in the symptoms of thrush.

For a complete list of side effects, please refer to the individual drug
monographs.

Read more

List of First generation cephalosporins:


Filter by:

View by: Brand | Generic


Drug Name Reviews Avg. Ratings

Duricef (Pro) 0 reviews 10


Generic name: cefadroxil

Velosef 0 reviews 10
Generic name: cephradine

Kefzol 0 reviews 9.0


Generic name: cefazolin

Keflex (Pro) 69 reviews 7.9


Generic name: cephalexin

Ancef (Pro) 0 reviews 6.5


Generic name: cefazolin

Biocef 0 reviews Add rating


Generic name: cephalexin

Panixine
Generic name: cephalexin

What are Fourth generation


cephalosporins?
Cephalosporins are a large group of antibiotics derived from the
mold Acremonium (previously called Cephalosporium). This mold yielded three
main compounds, historically called Cephalosporin N and C, and P, from which
the first cephalosporins were derived.

Cephalosporins are bactericidal (kill bacteria) and work in a similar way to


penicillins. They bind to and block the activity of enzymes responsible for making
peptidoglycan, an important component of the bacterial cell wall. They are called
broad-spectrum antibiotics because they are effective against a wide range of
bacteria.

Since the first cephalosporin was discovered in 1945, scientists have been
improving the structure of cephalosporins to make them more effective against a
wider range of bacteria. Each time the structure changes, a new "generation" of
cephalosporins are made. So far there are five generations of cephalosporins. All
cephalosporins start with cef, ceph, or kef. Note that this classification system is
not used consistently from country to country.

Fourth generation cephalosporins refer to the fourth group of cephalosporins


discovered. They are structurally related to third-generation cephalosporins but
possess an extra ammonium group, which allows them to rapidly penetrate
through the outer membrane of Gram-negative bacteria, enhancing their activity.
They are also active against β-lactamase producing Enterobacteriaceae which may
inactivate third-generation cephalosporins.

Some fourth-generation cephalosporins have excellent activity against gram-


positive bacteria such as methicillin-susceptible staphylococci, penicillin-
resistant pneumococci and viridans group streptococci.

Cefepime is the only fourth generation cephalosporin available in the United


States. Cefpirome is available overseas.

List of Fourth generation cephalosporins:


Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Maxipime (Pro)
Generic name: cefepime
1. Drug Classes

2. Anti-infectives
3. Cephalosporins

4. Next Generation Cephalosporins


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Next generation cephalosporins


Written by C. Fookes, BPharm on Jul 26, 2018

Other names: fifth generation cephalosporins, next-generation cephalosporins

What are Next generation cephalosporins?


Cephalosporins are a large group of antibiotics derived from the
mold Acremonium (previously called Cephalosporium). Cephalosporins are
bactericidal (kill bacteria) and work in a similar way to penicillins. They bind to
and block the activity of enzymes responsible for making peptidoglycan, an
important component of the bacterial cell wall. They are called broad-spectrum
antibiotics because they are effective against a wide range of bacteria.

Since the first cephalosporin was discovered in 1945, scientists have been
improving the structure of cephalosporins to make them more effective against a
wider range of bacteria. Each time the structure changes, a new "generation" of
cephalosporins are made. So far there are five generations of cephalosporins.
Next generation cephalosporins were the fifth generation of cephalosporins to be
developed.

What are next generation cephalosporins


used for?
Next generation cephalosporins have activity against multi-resistant
Staphylococcus aureus (MRSA), gram-positive bacteria and some gram-negative
bacteria. Ceftaroline is currently the only next-generation cephalosporin
available in the United States. In adults and children aged two years and older it
is approved to treat:

 Pneumonia that is acquired in the community (not in hospital)


 Skin and skin structure infections.

What are the differences between next


generation cephalosporins?
Ceftaroline is currently the only next-generation cephalosporin available in the
United States. It is active against methicillin-resistant Staphylococcus
aureus (MRSA) and gram-positive bacteria. It also retains the activity of the later-
generation cephalosporins and is effective against susceptible gram-negative
bacteria.

Generic name Brand name examples

ceftaroline Teflaro

Are next generation cephalosporins safe?


Next generation cephalosporins are generally safe, with low toxicity and good
efficacy against susceptible bacteria.

Allergic reactions have been reported with all cephalosporins including


ceftaroline and symptoms may include a rash, hives (urticaria), swelling, or
rarely, anaphylaxis. Up to 10% of people with a history of penicillin allergy will
also be allergic to cephalosporins.

A positive Coombs test (a test that checks your blood for antibodies that attack
red blood cells) has been reported in up to 18% of children and 11% of adults
taking ceftaroline. This may be associated with red blood cell hemolysis and
drug-induced hemolytic anemia should be suspected if anemia develops during
or after treatment.
Rarely, some people may develop a super-infection due to overgrowth of a
naturally occurring bacterium called Clostridium difficile, following use of any
antibiotic, including cephalosporins. Symptoms may include severe diarrhea.

Rarely, seizures have been reported with ceftaroline; the risk may be greatest in
those with kidney disease.

For a complete list of severe side effects, please refer to the ceftaroline drug
monograph.

What are the side effects of next generation


cephalosporins?
Ceftaroline generally causes few side effects. The most common side effects
reported include:

 Abdominal pain
 Constipation
 Diarrhea
 Dyspepsia
 A headache
 Insomnia
 Itchy skin
 Gastritis
 Nausea
 Rash
 Vomiting.

Transient increases in liver enzymes have also been reported

For a complete list of side effects, please refer to the ceftaroline drug
monograph.

List of Next generation cephalosporins:


Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Teflaro (Pro)
Generic name: ceftaroline

What are second generation cephalosporins


used for?
Second generation cephalosporins may be used to treat the following types of
infections when caused by susceptible strains of bacteria:

 Bone and joint infections


 Gynecological infections
 Intra-abdominal infections
 Lower respiratory tract infections
 Skin and skin structure infections
 Urinary tract infections

Cephalosporins are not usually used as a first-choice antibiotic. They tend to be


reserved for use when other antibiotics (often penicillins) cannot be used.

What are the differences between second


generation cephalosporins?
Second generation cephalosporins have activity against gram-negative aerobes
such as Morganella morganii, Neisseria gonorrhoeae (non-penicillinase producing
strains), Haemophilus influenzae, Klebsiella species, and Escherichia coli; gram-
positive aerobes such as Streptococcus pneumoniae, Staphylococcus
aureus, S. epidermidis and S. pyrogenes; and several types of anaerobes.
Some bacteria, such as most strains
of Pseudomonas aeruginosa and Acinetobacter species, are resistant to second
generation cephalosporins.

Second-generation cephalosporins are more active against gram-negative


bacteria than first generation cephalosporins

Generic name Brand name examples

cefotetan Cefotan

cefoxitin Mefoxin

cefprozil Cefzil

cefuroxime Ceftin, Zinacef

loracarbef Discontinued

Are second generation cephalosporins safe?


Second generation cephalosporins are generally safe, with low toxicity and good
efficacy against susceptible bacteria.

Allergic reactions have been reported with all cephalosporins including second
generation cephalosporins and symptoms may include a rash, hives (urticaria),
swelling, or rarely, anaphylaxis. Up to 10% of people with a history of penicillin
allergy will also be allergic to cephalosporins.

Drug-induced hemolytic anemia has been associated with the use of some
cephalosporins, including second generation cephalosporins; suspect and
investigate further if anemia develops during or after treatment.
Rarely, some people may develop a super-infection due to overgrowth of a
naturally occurring bacterium called Clostridium difficile, following use of any
antibiotic, including cephalosporins. Symptoms may include severe diarrhea.

Rarely, seizures have been reported with cephalosporins; the risk may be
greatest in those with kidney disease.

For a complete list of severe side effects, please refer to the individual drug
monographs.

What are the side effects of second


generation cephalosporins?
Second generation cephalosporins generally cause few side effects. The most
common side effects reported include:

 Abdominal pain
 Diarrhea
 Nausea
 Rash
 Vomiting.

Transient increases in liver enzymes have also been reported

For a complete list of side effects, please refer to the individual drug
monographs.

List of Second generation cephalosporins:


Filter by:

View by: Brand | Generic


Drug Name Reviews Avg. Ratings

Lorabid (Pro) 1 review 9.0


Generic name: loracarbef

Cefotan (Pro) 0 reviews 8.0


Generic name: cefotetan

Zinacef (Pro) 0 reviews 8.0


Generic name: cefuroxime

Ceftin (Pro) 43 reviews 7.4


Generic name: cefuroxime

Cefzil (Pro) 11 reviews 6.3


Generic name: cefprozil

Lorabid Pulvules 0 reviews Add rating


Generic name: loracarbef

Mefoxin (Pro)
Generic name: cefoxitin

What are third-generation cephalosporins


used for?
Third generation cephalosporins may be used to treat the following types of
infections when caused by susceptible strains of bacteria:

 Bacteremia/septicemia
 Bone and joint infections
 Central nervous system infections
 Gynecological infections
 Intra-abdominal infections
 Lower respiratory tract infections
 Skin and skin structure infections
 Urinary tract infections.

Cephalosporins are not usually used as a first-choice antibiotic. They tend to be


reserved for use when other antibiotics (often penicillins) cannot be used.

What are the differences between third-


generation cephalosporins?
There are differences between third-generation cephalosporins with regards to
the bacteria they are effective against. No one third-generation cephalosporin
treats all infectious disease scenarios.

Cefotaxime and ceftizoxime (discontinued) offer the best gram-positive


coverage out of all the third-generation agents; ceftazidime and cefoperazone
(discontinued) are unique in that they provide antipseudomonal coverage.

Ceftriaxone has a long half-life which allows for once daily dosing and may be
used for the treatment of gonorrhea, pelvic inflammatory disease, and
epididymo-orchitis. It is also an alternative to penicillins for
suspected meningitis.

All the third-generation cephalosporins except for cefoperazone (discontinued)


penetrate cerebrospinal fluid.

Generic name Brand name examples

cefdinir Omnicef

cefditoren Spectracef

cefixime Suprax
Generic name Brand name examples

cefoperazone Discontinued

cefotaxime Claforan

cefpodoxime Generic

ceftazidime Fortaz, Tazicef

ceftibuten Cedax

ceftriaxone Generic

Are third generation cephalosporins safe?


Third generation cephalosporins are generally safe, with low toxicity and good
efficacy against susceptible bacteria.

Allergic reactions have been reported with all cephalosporins including third
generation cephalosporins and symptoms may include a rash, hives (urticaria),
swelling, or rarely, anaphylaxis. Up to 10% of people with a history of penicillin
allergy will also be allergic to cephalosporins.

Drug-induced hemolytic anemia has been associated with use of some


cephalosporins, including third generation cephalosporins; suspect and
investigate further if anemia develops during or after treatment.

Rarely, some people may develop a super-infection due to overgrowth of a


naturally occurring bacterium called Clostridium difficile, following use of any
antibiotic, including cephalosporins. Symptoms may include severe diarrhea.

Rarely, seizures have been reported with cephalosporins; the risk may be
greatest in those with kidney disease.
Cephalosporin should be given exactly as directed. Potentially life-threatening
arrhythmias have been reported following rapid bolus administration of
cefotaxime, a third generation cephalosporin.

For a complete list of severe side effects, please refer to the individual drug
monographs.

What are the side effects of third


generation cephalosporins?
Third generation cephalosporins generally cause few side effects. The most
common side effects reported include:

 Abdominal pain
 Diarrhea
 Injection site inflammation
 Itchy skin
 Nausea
 Rash
 Vomiting.

Transient increases in liver enzymes have also been reported.

For a complete list of side effects, please refer to the individual drug
monographs.

List of Third generation cephalosporins:


Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Cedax (Pro) 3 reviews 9.2


Drug Name Reviews Avg. Ratings

Generic name: ceftibuten

Rocephin (Pro) 91 reviews 8.6


Generic name: ceftriaxone

Claforan (Pro) 0 reviews 8.0


Generic name: cefotaxime

Vantin (Pro) 6 reviews 7.8


Generic name: cefpodoxime

Omnicef (Pro) 47 reviews 6.5


Generic name: cefdinir

Suprax (Pro) 8 reviews 6.3


Generic name: cefixime

Omnicef Omni-Pac 2 reviews 4.0


Generic name: cefdinir

Spectracef (Pro) 3 reviews 3.7


Generic name: cefditoren

Cefizox 0 reviews Add rating


Generic name: ceftizoxime

Cefobid 0 reviews Add rating


Generic name: cefoperazone

Ceptaz 0 reviews Add rating


Generic name: ceftazidime
Drug Name Reviews Avg. Ratings

Fortaz (Pro) 0 reviews Add rating


Generic name: ceftazidime

Tazicef (Pro)
Generic name: ceftazidime

1. Reference

2. Antibiotics
Print Share

Antibiotics Guide
Medically reviewed by L. Anderson, PharmD Last updated on Jun 11, 2019.

 Care Notes
 Medication List
 Q&A

When To Use|When NOT To Use|Top 10 Infections Treated|Top 10 Generic


Drugs|Top 10 Brand Drugs|Antibiotic Class Types|OTC Options |More
Resources

Taking Antibiotics
You’ve most likely taken an antibiotic or anti-infective at least once in your
lifetime. From treatments for painful strep throat or ear infections as a child, to
burning urinary tract infections or itchy skin infections as an adult, antibiotics are
one of the most highly utilized and important medication classes we have in
medicine.

Understanding the vast world of antibiotics and anti-infectives is no easy


task. Anti-infectives are a large class of drugs that cover a broad range of
infections, including fungal, viral, bacterial, and even protozoal infections.
 Athletes foot? That’s a common fungal infection.
 HIV? Antiviral medications are always needed.
 Bladder infection? Yes, that may need a common oral antibiotic.
 Head lice? A topical anti-parasitic can alleviate the itching.

There is no one type of antibiotic that cures every


infection. Antibiotics specifically treat infections caused by bacteria, such as
Staph., Strep., or E. coli., and either kill the bacteria (bactericidal) or keep it from
reproducing and growing (bacteriostatic). Antibiotics do not work against
any viral infection.

When To Use Antibiotics


Antibiotics are specific for the type of bacteria being treated and, in general,
cannot be interchanged from one infection to another. When antibiotics are used
correctly, they are usually safe with few side effects.

However, as with most drugs, antibiotics can lead to side effects that may range
from being a nuisance to serious or life-threatening. In infants and the elderly, in
patients with kidney or liver disease, in pregnant or breastfeeding women, and in
many other patient groups antibiotic doses may need to be adjusted based upon
the specific characteristics of the patient, like kidney or liver function, weight, or
age. Drug interactions can also be common with antibiotics. Health care
providers are able to assess each patient individually to determine the correct
antibiotic and dose.

When NOT To Use Antibiotics


Antibiotics are not the correct choice for all infections. For example, most sore
throats, cough and colds, flu or acute sinusitis are viral in origin (not bacterial)
and do not need an antibiotic. These viral infections are “self-limiting”, meaning
that your own immune system will usually kick in and fight the virus off. In fact,
using antibiotics for viral infections can increase the risk for antibiotic resistance,
lower the options for future treatments if an antibiotic is needed, and put a
patient at risk for side effects and extra cost due to unnecessary drug treatment.
Antibiotic resistant bacteria cannot be fully inhibited or killed by an antibiotic,
even though the antibiotic may have worked effectively before the resistance
occurred. Don't share your antibiotic or take medicine that was prescribed for
someone else, and don't save an antibiotic to use the next time you get sick.

To better understand antibiotics, it’s best to break them down into common
infections, common antibiotics, and the top antibiotic classes as listed in
Drugs.com.

Top 10 List of Common Infections Treated


with Antibiotics
1. Acne
2. Bronchitis
3. Conjunctivitis (Pink Eye)
4. Otitis Media (Ear Infection)
5. Sexually Transmitted Diseases (STD’s)
6. Skin or Soft Tissue Infection
7. Streptococcal Pharyngitis (Strep Throat)
8. Traveler’s diarrhea
9. Upper Respiratory Tract Infection
10. Urinary Tract Infection (UTI)

Top 10 List of Generic Antibiotics


1. amoxicillin
2. doxycycline
3. cephalexin
4. ciprofloxacin
5. clindamycin
6. metronidazole
7. azithromycin
8. sulfamethoxazole and trimethoprim
9. amoxicillin and clavulanate
10. levofloxacin
Top 10 List of Brand Name Antibiotics
1. Augmentin
2. Flagyl, Flagyl ER
3. Amoxil
4. Cipro
5. Keflex
6. Bactrim, Bactrim DS
7. Levaquin
8. Zithromax
9. Avelox
10. Cleocin

Top 10 List of Antibiotic Classes (Types of


Antibiotics)
1. Penicillins
2. Tetracyclines
3. Cephalosporins
4. Quinolones
5. Lincomycins
6. Macrolides
7. Sulfonamides
8. Glycopeptides
9. Aminoglycosides
10. Carbapenems

Most antibiotics fall into their individual antibiotic classes. An antibiotic class is a
grouping of different drugs that have similar chemical and pharmacologic
properties. Their chemical structures may look comparable, and drugs within the
same class may kill the same or related bacteria.

However, it is important not to use an antibiotic for an infection unless your


doctor specifically prescribes it, even if it's in the same class as another drug you
were previously prescribed. Antibiotics are specific for the kind of bacteria they
kill. Plus, you would need a full treatment regimen to effectively cure your
infection, so don't use or give away leftover antibiotics.

1. Penicillins
Another name for this class is the beta-lactam antibiotics, referring to their
structural formula. The penicillin class contains five groups of
antibiotics: aminopenicillins, antipseudomonal penicillins, beta-lactamase
inhibitors, natural penicillins, and the penicillinase resistant penicillins.

Common antibiotics in the penicillin class include:

Generic Brand Name Examples

amoxicillin Amoxil

amoxicillin and clavulanate Augmentin, Augmentin ES-600, Augmentin XR

ampicillin Unasyn

dicloxacillin Dynapen (discontinued)

oxacillin Bactocill (discontinued)

penicillin V potassium PC Pen VK (discontinued)

Certain penicillinase-resistant penicillins (such as oxacillin or dicloxacillin) are


inherently resistant to certain beta-lactamase enzymes by themselves. Others, for
example, amoxicillin or ampicillin have greater antibacterial activity when they
are combined with a beta-lactamase inhibitor like clavulanate, sulbactam, or
tazobactam.

View all penicillin drugs


2. Tetracyclines
Tetracyclines are broad-spectrum against many bacteria and treat conditions
such as acne, urinary tract infections (UTIs), intestinal tract infections, eye
infections, sexually transmitted diseases, periodontitis (gum disease), and other
bacterial infections. The tetracycline class contains drugs such as:

Generic Brand Name Examples

demeclocycline Declomycin

doxycycline Adoxa, Doryx, Doxy 100, Oracea, Vibramycin

eravacycline Xerava

minocycline Dynacin, Minocin, Solodyn

omadacycline Nuzyra

tetracycline Panmycin, Sumycin

View all tetracycline drugs

3. Cephalosporins
There are five generations of cephalosporins, with increasing expanded
coverage across the class to include gram-negative infections. Newer generations
with updated structures are developed to allow wider coverage of certain
bacteria. Cephalosporins are bactericidal (kill bacteria) and work in a similar way
as the penicillins. Cephalosporins treat many types of infections, including strep
throat, ear infections, urinary tract infections, skin infections, lung infections, and
meningitis. Common medications in this class include:
Generic Brand Name Examples

cefaclor Ceclor (brand discontinued)

cefdinir Omnicef (discontinued)

cefotaxime Claforan

ceftazidime Avycaz, Fortaz, Tazicef

ceftriaxone Rocephin (discontinued)

cefuroxime Zinacef

The fifth generation (or next generation) cephalosporin known


as ceftaroline (Teflaro) is active against methicillin-resistant Staphylococcus
aureus (MRSA). Avycaz contains the the beta-lactamase inhibitor avibactam.

View all cephalosporin drugs

4. Quinolones
The quinolones, also known as the fluoroquinolones, are a synthetic, bactericidal
antibacterial class with a broad-spectrum of activity. The quinolones can be used
for difficult-to-treat urinary tract infections when other options are aren’t
effective, hospital-acquired pneumonia, bacterial prostatitis, and even anthrax or
plague.

The FDA has issued several strong warnings about this class due to potential
disabling side effects. Learn More: Fluoroquinolone Antibacterial Drugs for
Systemic Use: Drug Safety Communication - Warnings Updated Due to
Disabling Side Effects

Common drugs in the fluoroquinolone class include:


Generic Brand Name Examples

ciprofloxacin Cipro, Cipro XR

levofloxacin Levaquin

moxifloxacin Avelox

Several quinolones are also available in drop form to treat eye or ear infections.

View all quinolone drugs

5. Lincomycins
This class has activity against gram-positive aerobes and anaerobes (bacteria that
can live without oxygen), as well as some gram-negative anaerobes. The
lincomycin derivatives may be used to treat serious infections like pelvic
inflammatory disease, intra-abdominal infections, lower respiratory tract
infections, and bone and joint infections. Some forms are also used topically on
the skin to treat acne. These drugs include:

Generic Brand Name Examples

clindamycin Cleocin, Cleocin T, Evoclin

lincomycin Lincocin

View all lincomycin drugs

6. Macrolides
The macrolides can be use to treat community-acquired pneumonia, pertussis
(whooping cough), or for uncomplicated skin infections, among other susceptible
infections. Ketolides are a newer generation of antibiotic developed to overcome
macrolide bacterial resistance. Frequently prescribed macrolides are:

Generic Brand Name Examples

azithromycin Zithromax

clarithromycin Biaxin

erythromycin E.E.S., Ery-Tab, Eryc

View all macrolide drugs

7. Sulfonamides
Sulfonamides are effective against some gram-positive and many gram-negative
bacteria, but resistance is widespread. Uses for sulfonamides include urinary tract
infections (UTIs), treatment or prevention of pneumocystis pneumonia, or ear
infections (otitis media). Familiar names include:

Generic Brand Name Examples

sulfamethoxazole and trimethoprim Bactrim, Bactrim DS, Septra

sulfasalazine Azulfidine

sulfisoxazole (product discontinued) Eryzole (discontinued), Gantrisin (discontinued)

View all sulfonamides drugs

8. Glycopeptide Antibiotics
Members of this group may be used for treating methicillin-
resistant staphylococcus aureus (MRSA) infections, complicated skin infections, C.
difficile-associated diarrhea, and enterococcal infections such as endocarditis
which are resistant to beta-lactams and other antibiotics. Common drug names
include:

Generic Brand Name Examples

dalbavancin Dalvance

oritavancin Orbactiv

telavancin Vibativ

vancomycin Firvanq, Vancocin

View all glycopeptide drugs

9. Aminoglycosides
Aminoglycosides inhibit bacterial synthesis by binding to the 30S ribosome and
act rapidly as bactericidal antibiotics (killing the bacteria). These drugs are usually
given intravenously (in a vein through a needle). Common examples in this class
are:

Generic Brand Name Examples

gentamicin Garamycin (discontinued), Genoptic

tobramycin TOBI, Tobradex, Tobrex

amikacin Amikin
View all aminoglycoside drugs

10. Carbapenems
These injectable beta-lactam antibiotics have a wide spectrum of bacteria-killing
power and may be used for moderate to life-threatening bacterial infections like
stomach infections, pneumonias, kidney infections, multidrug-resistant hospital-
acquired infections and many other types of serious bacterial illnesses. They are
often saved for more serious infections or used as "last-line" agents to help
prevent resistance. Members of this class include:

Generic Brand Name Examples

imipenem and cilastatin Primaxin

meropenem Merrem

doripenem Doribax (discontinued)

ertapenem Invanz

View all carbapenems drugs

Are There Any Over-the-Counter


Antibiotics?
Over-the-counter (OTC) oral antibiotics are not approved in the U.S. A bacterial
infection is best treated with a prescription antibiotic that is specific for the type
of bacteria causing the infection. Using a specific antibiotic will increase the
chances that the infection is cured and help to prevent antibiotic resistance. In
addition, a lab culture may need to be performed to pinpoint the bacteria and to
help select the best antibiotic. Taking the wrong antibiotic -- or not enough --
may worsen the infection and prevent the antibiotic from working the next time.
There are a few over-the-counter topical antibiotics that can be used on the
skin. Some products treat or prevent minor cuts, scrapes or burns on the skin that
may get infected with bacteria. These are available in creams, ointments, and
even sprays.

Common OTC topical antibiotics:


 Neosporin (bacitracin, neomycin, polymyxin B)
 Polysporin (bacitracin, polymyxin B)
 Triple antibiotic, generic (bacitracin, neomycin, polymyxin B)
 Neosporin + Pain Relief Ointment (bacitracin, neomycin, polymyxin B,
pramoxine)

There are some OTC antibacterials for treating acne, too. They contain the
antibacterial benzoyl peroxide, which also has mild drying effect for acne. Many
products are found on the pharmacy shelves as gels, lotions, solutions, foams,
cleaning pads, and even facial scrubs.

Common OTC antibacterials for acne:

 Clearskin
 Oxy-10
 Proactiv

1. Drug Classes

2. Anti-infectives

3. Penicillins
Print Share

Penicillins
Medically reviewed by C. Fookes, BPharm Last updated on Apr 5, 2018.

What are Penicillins?


Penicillins are a type of antibiotic derived from Penicillium fungi. An antibiotic is a
type of medicine that inhibits the growth of, or kills, bacteria.

Penicillin G (also called benzylpenicillin) was discovered by accident in 1928.


Alexander Fleming, a Scottish physician-scientist was growing a type of bacteria
called Staphylococcus Aureus on an uncovered petri dish when it became
contaminated with mold spores. He observed that the areas of bacteria near the
mold were dying. He isolated the substance from the mold that was killing the
bacteria and called it penicillin.

Another naturally occurring penicillin, penicillin V was later isolated from the
same mold. All other penicillins are semi-synthetic (made by modifying the
structure of the original naturally occurring penicillins). Modification extends their
spectrum of activity, allows them to be taken orally, and increases their resistance
against penicillinase, an enzyme produced by some bacteria that inactivates
penicillin.

Penicillins work by preventing the cross linking of amino acid chains in the
bacterial cell wall. This does not affect pre-existing bacteria, but newly produced
bacterial cells have weak cell walls that easily rupture.

What are penicillins used for?


Penicillins may be used to treat a wide range of infections caused by susceptible
bacteria, such as:

 Dental abscess
 Ear infections (eg, otitis media)
 Gonorrhea
 Pneumonia
 Respiratory tract infections
 Rheumatic fever
 Scarlet fever
 Skin infections
 Urinary tract infections.
What are the differences between
penicillins?
The natural penicillins (penicillin G and penicillin V) are only active against
gram-positive bacteria (see below for an explanation). Penicillin V is more acid-
resistant than penicillin G, which means it can be taken orally.

Modern semi-synthetic penicillins include ampicillin, carbenicillin (discontinued),


and oxacillin. These can be taken orally, have some degree of resistance to beta
lactamase, and are effective against some gram-negative bacteria. Most bacteria
can be classified as gram-positive or gram-negative based on differences in their
cell wall structure, which can be distinguished under a microscope using a type of
dye. One of the most important differences between these two types of bacteria
is that gram-positive bacteria are more susceptible to antibiotics while gram-
negative bacteria are more resistant to antibiotics.

Antipseudomonal penicillins, such as piperacillin and ticarcillin (discontinued) are


penicillins that have additional activity against some hard-to-kill types of gram-
negative bacteria such as Pseudomonas, Enterococcus and Klebsiella. They are
useful for urinary tract infections caused by susceptible bacteria because they
concentrate in the urine.

Some penicillins are combined with a beta-lactamase inhibitor. A beta-lactamase


inhibitor blocks the activity of beta-lactamase enzymes but tends to have little
antibiotic activity on its own. Some penicillins (such as oxacillin, dicloxacillin,
and nafcillin) are naturally resistant to certain beta-lactamases and are called
penicillinase-resistant penicillins. Others, such as amoxicillin, ampicillin,
and piperacillin can have their activity extended by combining them with a beta-
lactamase inhibitor. Clavulanate, sulbactam, and tazobactam are all beta-
lactamase inhibitors.

Common penicillins available in the U.S.


Aminopenicillins
Spectrum of activity:
 Most gram-positive bacteria, some gram-negative bacteria (such as E.
coli and H. influenzae).

Generic name Brand name examples

amoxicillin Amoxil, Moxatag

ampicillin Principen

Antipseudomonal penicillins
Spectrum of activity:

 Most gram-positive and gram-negative bacteria


 Antipseudomonal and antiprotozoal activity
 Usually given with a beta lactamase.

Generic name Brand name examples

piperacillin Pipracil

Beta-lactamase inhibitors

Spectrum of activity:

 Effective against most gram-positive and gram-negative bacteria including


those that produce beta-lactamases
(eg, bacteroides sp., enterococcus sp., staphylococcus sp.)

Generic name Brand name examples

amoxicillin/clavulanate Augmentin, Amoclan


Generic name Brand name examples

ampicillin/sulbactam Unasyn

piperacillin/tazobactam Zosyn

Natural penicillins

Spectrum of activity:

 Effective against most gram-positive bacteria and a limited number of


gram-negative bacteria.

Generic name Brand name examples

penicillin g benzathine Bicillin L-A

penicillin v Penicillin VK

Penicillinase-resistant penicillins
Spectrum of activity:

 Effective against most gram-positive and gram-negative bacteria


 Naturally resistant to beta-lactamase.

Generic name Brand name examples

dicloxacillin Dycill

nafcillin Unipen

oxacillin Bactocill
Are penicillins safe?
Penicillins are generally safe, with low toxicity and good efficacy against
susceptible bacteria.

Many people believe that they are allergic to penicillin. However, true penicillin
allergy is rare, and only occurs in 0.01-0.05% of people who take penicillin.
Symptoms may include nausea, vomiting, itchy skin, rash, wheezing, swelling
around the throat, and respiratory collapse.

What are the side effects of penicillins?


Penicillins generally cause few side effects. The most common side effects
reported include abdominal pain, headache, rash, diarrhea, and taste perversion.

Penicillins may cause anaphylaxis in those allergic to penicillin, but the overall
incidence of anaphylaxis is rare (0.01-0.05%).

Rarely, some people may develop a super-infection due to overgrowth of a


naturally occurring bacterium called Clostridium difficile, following use of any
antibiotic, including penicillins. Symptoms may include severe diarrhea.

Uncommonly, an overgrowth of the yeast, Candida albicans, may occur following


penicillin use, resulting in the symptoms of thrush.

1. Drug Classes

2. Anti-infectives

3. Tetracyclines
Print Share

Tetracyclines
Written by C. Fookes, BPharm on Jun 8, 2018
What are Tetracyclines?
Tetracyclines are a class of antibiotics that may be used to treat infections caused
by susceptible microorganisms such as gram positive and gram negative bacteria,
chlamydiae, mycoplasmata, protozoans, or rickettsiae.

They were discovered in the 1940s and the first tetracyclines were obtained or
derived from Streptomyces bacteria.

Tetracyclines inhibit protein synthesis in the microbial RNA (an important


molecule that acts as a messenger for DNA). They are primarily bacteriostatic
which means that they prevent bacteria from multiplying but don't necessarily kill
them.

Although tetracyclines are still widely used in human and veterinary medicine, the
emergence of bacterial resistance has limited their effectiveness and is of major
concern.

What are tetracyclines used for?


Tetracyclines are used widely in both human and veterinary medicine; for
example, tetracyclines have been used:

 For the prevention of malaria


 For the treatment of moderate-to-severe acne or rosacea
 To treat anthrax
 To treat infections of the eye, gastrointestinal tract, genitourinary tract,
gums, respiratory tract, and skin
 To treat infections caused by lice, mites, or ticks (such as Rocky Mountain
spotted fever, typhus fever)
 To treat infections caused by Campylobacter, Chlamydiae, Yersinia
pestis (plague), Vibrio cholerae (cholera) and other atypical organisms
 To treat respiratory tract infections caused by Mycoplasma pneumoniae
 As a growth promoter in animals.

Because many strains of microorganisms are now resistant to some tetracyclines,


culture and susceptibility testing is recommended before beginning treatment.
Doxycycline is a tetracycline that may be considered when penicillin is
contraindicated.

What are the differences between


tetracyclines?
Although tetracyclines all work in the same way, there are differences between
the four tetracyclines (demeclocycline, doxycycline, minocycline,
and tetracycline) that are available in the U.S.

Doxycycline is the most widely prescribed tetracycline because it has the


advantage of once or twice daily dosing, availability as both an oral and an IV
preparation, and it may be taken with food without significant disruption to its
absorption. It is also less likely than other tetracyclines to cause photosensitivity
or to bind to calcium and cause tooth discoloration or bony growth
retardation. Conversely, there has been a resurgence in use of IV minocycline
because resistance appears lower with minocycline compared with other
tetracyclines.

Generic name Brand name examples

demeclocycline Declomycin

doxycycline Adoxa, Doryx, Vibramycin

minocycline Dynacin, Minocin, Solodyn

tetracycline Ala-tet, Tetracap

Are tetracyclines safe?


Tetracyclines are considered safe when used at the recommended dosages for
the recommended duration of time. However, tetracyclines have been associated
with serious side effects, such as:
 Tooth discoloration (yellow-gray-brown) and bony growth retardation
when given during tooth or bone development (last half of pregnancy,
infancy, and during childhood up until the age of 8 years)
 Clostridium difficile associated diarrhea (CDAD). CDAD ranges in severity
from mild diarrhea to fatal colitis and has been associated with nearly all
antibacterial agents, not just tetracyclines
 Intracranial hypertension (increased pressure within the brain) has been
associated with tetracycline use. Symptoms include a headache; double,
blurred, or loss of vision. Women of childbearing age who
are overweight or who have a history of intracranial hypertension are most
at risk. Coadministration of isotretinoin increases the risk and is
contraindicated
 Toxicity to a developing fetus (tetracyclines can slow skeletal
development). Tetracyclines should only be used in pregnancy if the
benefits outweigh the risk
 Drug Rash with Eosinophilia and Systemic Symptoms (DRESS). Symptoms
include widespread rash, fever, and swollen lymph nodes, and is potentially
fatal. Discontinue the tetracycline immediately.

For a complete list of severe side effects, please refer to the individual drug
monographs.

What are the side effects of tetracyclines?


The following are some of the side effects that have been reported with
tetracyclines:

 Gastrointestinal effects such as acid reflux, diarrhea, nausea, vomiting,


stomach cramps, or loss of appetite
 A headache
 An increase in some laboratory values (such as blood urea nitrogen [BUN])
particularly in people with impaired renal function. This does not appear to
happen with doxycycline
 Photosensitivity reactions (such as an exaggerated sunburn reaction).
Rarely occurs with minocycline
 Pigmentation or discoloration of the skin and mucous membranes
(minocycline only)
 Skin rash or itching
 Sore mouth or tongue
 Vaginal itching or discharge.

Demeclocycline has also been associated with increased thirst, increased


frequency of urination and unusual tiredness. Minocycline has been associated
with dizziness, light-headedness, and unsteadiness. Tetracyclines may also cause
darkening or discoloration of the tongue but this is usually temporary.

For a complete list of side effects, please refer to the individual drug
monographs.

Read more

List of Tetracyclines:
Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ra

Adoxa TT 0 reviews 1
Generic name: doxycycline

Oraxyl 0 reviews 1
Generic name: doxycycline

Adoxa (Pro) 4 reviews 9


Generic name: doxycycline

Declomycin (Pro) 2 reviews 9


Generic name: demeclocycline

Dynacin (Pro) 2 reviews 9


Drug Name Reviews Avg. Ra

Generic name: minocycline

Oracea (Pro) 43 reviews 8


Generic name: doxycycline

Monodox (Pro) 33 reviews 7


Generic name: doxycycline

Minocin (Pro) 18 reviews 7


Generic name: minocycline

Doxy 100 (Pro) 18 reviews 7


Generic name: doxycycline

Vibramycin (Pro) 8 reviews 7


Generic name: doxycycline

Doryx (Pro) 65 reviews 7


Generic name: doxycycline

Solodyn (Pro) 100 reviews 7


Generic name: minocycline

Acticlate (Pro) 7 reviews 6


Generic name: doxycycline

Terramycin 0 reviews 5
Generic name: oxytetracycline

Achromycin V 0 reviews Add ra


Generic name: tetracycline

Actisite 0 reviews Add ra


Drug Name Reviews Avg. Ra

Generic name: tetracycline

Adoxa CK 0 reviews Add ra


Generic name: doxycycline

Ala-Tet 0 reviews Add ra


Generic name: tetracycline

Alodox 0 reviews Add ra


Generic name: doxycycline

Avidoxy 0 reviews Add ra


Generic name: doxycycline

Avidoxy DK 0 reviews Add ra


Generic name: doxycycline / salicylic acid

Brodspec 0 reviews Add ra


Generic name: tetracycline

Cleeravue-M 0 reviews Add ra


Generic name: minocycline

Minocin for Injection 0 reviews Add ra


Generic name: minocycline

Minolira (Pro) 0 reviews Add ra


Generic name: minocycline

Morgidox 0 reviews Add ra


Generic name: doxycycline

Myrac 0 reviews Add ra


Drug Name Reviews Avg. Ra

Generic name: minocycline

NutriDox Convenience Kit 0 reviews Add ra


Generic name: doxycycline / omega-3 polyunsaturated fatty acids

Nuzyra (Pro) 0 reviews Add ra


Generic name: omadacycline

Ocudox 0 reviews Add ra


Generic name: doxycycline

Panmycin 0 reviews Add ra


Generic name: tetracycline

Periostat (Pro) 0 reviews Add ra


Generic name: doxycycline

Seysara (Pro) 0 reviews Add ra


Generic name: sarecycline

Sumycin (Pro) 0 reviews Add ra


Generic name: tetracycline

Tetracap 0 reviews Add ra


Generic name: tetracycline

Tetracon 0 reviews Add ra


Generic name: tetracycline

Vibra-Tabs 1 review Add ra


Generic name: doxycycline

Xerava (Pro) 0 reviews Add ra


Drug Name Reviews Avg. Ra

Generic name: eravacycline

Ximino (Pro)
Generic name: minocycline

1. Drug Classes

2. Anti-infectives

3. Quinolones
Print Share

Quinolones
Written by C. Fookes, BPharm on Apr 12, 2018

Other names: fluoroquinolones

What are Quinolones?


Quinolones are a type of antibiotic. Antibiotics kill or inhibit the growth of
bacteria.

There are five different quinolone classes. In addition, another class of antibiotic,
called fluoroquinolones, were derived from quinolones by modifying their
structure with fluorine. Quinolones and fluoroquinolones have many things in
common, but also a few differences such as what organisms they are effective
against. Some people use the words quinolones and fluoroquinolones
interchangeably.

Quinolones and fluoroquinolones detrimentally affect the function of two


enzymes produced by bacteria, topoisomerase IV and DNA gyrase, so that they
can no longer repair DNA or help in its manufacture.
What are quinolones and fluoroquinolones
used for?
Quinolones and fluoroquinolones are considered broad-spectrum antibiotics.
This means that they are effective against a wide range of bacteria.

However, because of their risk of serious side effects, the FDA has advised that
they are not suitable for common conditions such as sinusitis, bronchitis, and
uncomplicated urinary tract infections, and should only be considered when
treatment with other, less toxic antibiotics, has failed.

Quinolones and fluoroquinolones may also be used to treat unusual infections


such as anthrax or plague. Doctors may also decide to use them for other types
of infection when other alternative treatment options have failed or cannot be
used.

What are the differences between


quinolones and fluoroquinolones?
Quinolones and fluoroquinolones differ in their activity against the two enzymes
produced by bacteria, topoisomerase IV and DNA gyrase. Those that are more
active against topoisomerase IV have more of an effect against gram-positive
bacteria, those that are active against DNA gyrase, are more active against gram-
negative bacteria. Newer fluoroquinolones tend to target these enzymes equally.

Quinolones and fluoroquinolones also differ in the way they are absorbed,
metabolized and excreted in the body.

Table: List of common quinolones and fluoroquinolones

Generic name Brand name examples

cinoxacin Discontinued in the U.S.


Generic name Brand name examples

ciprofloxacin Cipro, Proquin XR

delafloxacin Baxdela

gemifloxacin Factive

levofloxacin Levaquin

moxifloxacin Avelox

nalidixic acid Discontinued in the U.S.

norfloxacin Discontinued in the U.S.

ofloxacin Floxin

sparfloxacin Discontinued in the U.S.

Are quinolones and fluoroquinolones safe?


Quinolones and fluoroquinolones should be avoided in children under the age of
18 years unless they have a serious infection that cannot be treated with any
other antibiotic. This is because they can damage the weight-bearing joints in
children, and children are also more susceptible to other adverse effects of
quinolones and fluoroquinolones, including tendinitis and tendon rupture.

The FDA has some concerns about quinolones and fluoroquinolones and
considers them unsuitable for most common infections because they have been
associated with some serious effects, including tendinitis (inflammation of a
tendon) and tendon rupture. In addition, some people have reported peripheral
neuropathy (nerve pain in the fingers and toes) and central nervous system
effects such as agitation, attention problems, disorientation, memory
impairment, nervousness, and delirium while taking quinolones or
fluoroquinolones. They have also been associated with low blood sugar levels
(hypoglycemia). All quinolones and fluoroquinolones are required by the FDA to
carry safety warnings about these potentially serious side effects.

The risk of tendinitis and tendon rupture is increased in people over the age of
60, in those taking corticosteroids, or with a history of organ transplant. Previous
tendon disorders or strenuous activity may also increase risk.

Occasionally, liver damage and allergic reactions have occurred in people taking
quinolones or fluoroquinolones.

If any of these very severe side effects happen, the quinolone or fluoroquinolone
should be discontinued immediately, and all other quinolones and
fluoroquinolones avoided in the future.

What are the side effects of quinolones and


fluoroquinolones?
The most commonly reported side effects include diarrhea, nausea, abnormal
liver function tests, vomiting, and rash.

Quinolones and fluoroquinolones may also cause anxiety, insomnia, psychotic


reactions, nerve pain or a loss of feeling in the extremities, electrocardiogram
(ECG) abnormalities, increased sensitivity to light and other effects.

In people with myasthenia gravis, they may exacerbate muscle weakness and
may trigger seizures or increase the risk of having a seizure.

In people with diabetes, quinolones and fluoroquinolones may affect blood


glucose levels requiring extra monitoring.

Quinolones and fluoroquinolones increase the sensitivity of the skin to the sun
and may cause photo-sensitivity reactions and severe sunburn on exposed areas
of skin.
Quinolones and fluoroquinolones are not suitable for people with myasthenia
gravis, certain heart rhythm disturbances, or children and adolescents under the
age of 18 (unless the infection cannot be treated by another antibiotic).

Read more

List of Quinolones:
Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Avelox I.V. (Pro) 1 review 10


Generic name: moxifloxacin

Maxaquin 0 reviews 10
Generic name: lomefloxacin

Tequin 0 reviews 8.7


Generic name: gatifloxacin

Noroxin (Pro) 2 reviews 8.5


Generic name: norfloxacin

Floxin (Pro) 2 reviews 7.8


Generic name: ofloxacin

Avelox (Pro) 155 reviews 6.8


Generic name: moxifloxacin

NegGram 1 review 6.0


Generic name: nalidixic acid
Drug Name Reviews Avg. Ratings

Cipro (Pro) 283 reviews 5.7


Generic name: ciprofloxacin

Baxdela (Pro) 1 review 5.5


Generic name: delafloxacin

Levaquin (Pro) 376 reviews 5.4


Generic name: levofloxacin

Proquin XR (Pro) 1 review 5.0


Generic name: ciprofloxacin

Cipro I.V. 3 reviews 4.3


Generic name: ciprofloxacin

Factive (Pro) 9 reviews 3.8


Generic name: gemifloxacin

Cipro XR (Pro) 2 reviews 2.0


Generic name: ciprofloxacin

Cinobac 0 reviews Add rating


Generic name: cinoxacin

Trovan 0 reviews Add rating


Generic name: trovafloxacin

Zagam
Generic name: sparfloxacin

What are Lincomycin derivatives?


Lincomycin derivatives are a small group of antibiotics that inhibit synthesis of
bacterial proteins, essential for bacteria to survive. Lincomycin derivatives are
reserved for treatment of infections due to susceptible strains of pneumococci,
staphylococci and streptococci. One derivative is also indicated for treatment of
Plasmodium falciparum (malaria).

List of Lincomycin derivatives:


Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Lincocin (Pro) 1 review 10


Generic name: lincomycin

Cleocin HCl 3 reviews 8.5


Generic name: clindamycin

Cleocin (Pro) 16 reviews 6.1


Generic name: clindamycin

Cleocin Pediatric (Pro) 0 reviews Add rating


Generic name: clindamycin

Cleocin Phosphate (Pro)


Generic name: clindamycin
1. Drug Classes

2. Anti-infectives

3. Macrolide Derivatives
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Macrolide derivatives
What are Macrolide derivatives?
Macrolide derivatives are either macrolide antibiotics or other antibiotics related
to macrolides.

Macrolides are a class of antibiotics found in streptomycetes. They are natural


lactones with a large ring, consisting of 14 to 20 atoms. Macrolides bind to the
50S subunit of the bacterial ribosome and inhibit ribosomal translocation, leading
to inhibition of bacterial protein synthesis. Their action is primarily bacteriostatic
but may be bactericidal at high concentrations, or depending on the type of
microorganism.

What are Ketolides?


Ketolides are a new generation of macrolide antibiotics designed to overcome
issues with bacterial resistance to macrolides. They are semi-synthetic antibiotics
derived from erythromycin (macrolide antibiotic) and the changes give ketolides
a broader spectrum of activity.

Ketolides bind to the bacterial 50S ribosomal subunit and inhibit RNA-dependent
protein synthesis. They are bacteriostatic at low concentrations and bactericidal
at high concentration, so basically exhibit concentration dependent killing.

Ketolides have good antibacterial activity against Gram-positive bacteria such as


those that cause respiratory tract infections.

List of Ketolides:
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Drug Name Reviews Avg. Ratings

Ketek (Pro) 0 reviews Add rating


Generic name: telithromycin
Drug Name Reviews Avg. Ratings

Ketek Pak
Generic name: telithromycin

What are Macrolides?


Macrolides are a class of antibiotics derived from Saccharopolyspora
erythraea (originally called Streptomyces erythreus), a type of soil-borne bacteria.

Macrolides inhibit protein synthesis in bacteria by reversibly binding to the P site


of the 50S unit of the ribosome. Macrolides mainly affect gram-positive cocci and
intracellular pathogens such as mycoplasma, chlamydia, and legionella.
Erythromycin was the first macrolide discovered; other macrolides include
azithromycin, clarithromycin, and roxithromycin.

Their action is primarily bacteriostatic but may be bactericidal at high


concentrations, or depending on the type of microorganism.

List of Macrolides:
Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

E.E.S.-400 1 review 10
Generic name: erythromycin

Zmax (Pro) 0 reviews 8.0


Generic name: azithromycin

Zithromax (Pro) 121 reviews 7.4


Generic name: azithromycin

Biaxin XL 9 reviews 7.2


Generic name: clarithromycin
Drug Name Reviews Avg. Ratings

Erythrocin (Pro) 3 reviews 7.2


Generic name: erythromycin

Azithromycin Dose Pack 55 reviews 7.0


Generic name: azithromycin

Ery-Tab (Pro) 1 review 7.0


Generic name: erythromycin

Dificid (Pro) 5 reviews 6.8


Generic name: fidaxomicin

Biaxin (Pro) 85 reviews 6.4


Generic name: clarithromycin

E.E.S. Granules (Pro) 0 reviews Add rating


Generic name: erythromycin

Eryc (Pro) 0 reviews Add rating


Generic name: erythromycin

EryPed (Pro) 0 reviews Add rating


Generic name: erythromycin

Erythrocin Lactobionate 0 reviews Add rating


Generic name: erythromycin

Ilosone 0 reviews Add rating


Generic name: erythromycin

PCE Dispertab (Pro)


Generic name: erythromycin
1. Drug Classes

2. Anti-infectives

3. Sulfonamides
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Sulfonamides
Written by C. Fookes, BPharm on Jun 21, 2018

Other names: sulfa drugs, sulphonamides

What are Sulfonamides?


Sulfonamides (sulphonamides) are a group of man-made (synthetic) medicines
that contain the sulfonamide chemical group. They may also be called sulfa
drugs.

Many people use the term sulfonamide imprecisely to refer only to antibiotics
that have a sulfonamide functional group in their chemical structure. However,
there are several non-antibiotic sulfonamides that have been developed by
exploiting observations made during the clinical evaluation of the antibiotic
sulfonamides. These are used for a range of conditions such as diabetes and pain
relief.

Sulfanilamide was the first sulfonamide developed in 1906, although it was not
used as an antimicrobial agent until the late 1930s. Sulfonamide antimicrobials
are bacteriostatic (stop bacteria from reproducing but don't necessarily kill them)
and work by interfering with the synthesis of folic acid in bacteria, which is
essential for nucleic acid formation and ultimately DNA and RNA. Humans obtain
folic acid from their diet, but bacteria need to synthesize it. Sulfonamide
antimicrobials may be combined with trimethoprim to make them bactericidal
(kill bacteria), because trimethoprim acts on a different enzyme in the folic acid
synthesis pathway.

Non-antibiotic sulfonamides are thought to have anti-inflammatory or


immunomodulatory properties although the exact way they work in some
conditions is not known.

What are sulfonamides used for?


Sulfonamides represent a diverse range of medicines with a diverse range of
actions. Examples of some conditions that may be treated with sulfonamides
include:
 Bacterial infections: eg, sulfamethoxazole/trimethoprim, sulfisoxazole
 Crohn’s disease: eg, sulfasalazine
 Diabetes: eg, glyburide, tolbutamide
 Fluid retention: eg, chlorothiazide, furosemide, hydrochlorothiazide
 Gout: eg, probenecid
 High blood pressure: eg, chlorothiazide, hydrochlorothiazide
 Pain and inflammation: eg, celecoxib
 Rheumatoid arthritis: eg, sulfasalazine
 Ulcerative colitis: eg, sulfasalazine.

What are the differences between


sulfonamides?
Sulfonamide antibiotics have an N4 amine group in their structure which is
thought to contribute to their higher incidence of allergic-type reactions. Non-
antibiotic sulfonamides lack this structure.

Sulfonamide antibiotics

Oral sulfonamides are rapidly excreted and very soluble in urine and are
commonly used to treat infections of the urinary tract.

Generic name Brand name examples

sulfacetamide topical Klaron, Ovace

sulfadiazine Generic only

sulfamethoxazole/trimethoprim Bactrim, Septa, SMZ-TMP

sulfisoxazole Gantrisin Pediatric, Truxazole

Non-antibiotic sulfonamides
Many classes of drugs contain a sulfonamide structure including carbonic
anhydrase inhibitors; sulfonylureas; and thiazide, thiazide-like and loop
diuretics.

Generic name Brand name examples

acetazolamide Diamox

bumetanide Bumex

celecoxib Celebrex

chlorothiazide Diuril

chlorthalidone Thalitone

dapsone Generic

dorzolamide opthalmic Trusopt

furosemide Lasix

glibenclamide Not available in the U.S.

gliclazide Not available in the U.S.

glipizide Glucotrol

glyburide Micronase

hydrochlorothiazide (HCTZ) Aquazide H, Microzide

indapamide Lozol
Generic name Brand name examples

probenecid Benemid

sulfasalazine* Azulfidine, Sulfazine

sumatriptan Imitrex

tolbutamide Orinase, Tol-tab

*Sulfasalazine also has an antibacterial effect.

Are sulfonamides safe?


Sulfonamide-containing drugs are frequently implicated in allergic and non-
allergic reactions.

The term “sulfa allergy” (or “sulfur allergy”) most commonly refers to an
immunological response to sulfonamides, and it is a term that is often misused
and misinterpreted. It should not be confused with a sulphite allergy (sulphites
are substances used to preserve foods); nor with an allergy to the element
sulphur or sulphates (allergic reactions to these naturally occurring substances
are extremely rare). Non-antibiotic sulfonamides are thought to be less likely than
antibiotic sulfonamides to cause severe allergic reactions.

Sulfonamide allergic reactions affect 1.5-3% of the population but are 10 times
more likely in people with HIV. Management depends on the type and severity of
the reaction. Mild reactions can be treated with drug discontinuation and
antihistamine administration. More severe reactions may require topical or oral
steroids and possibly hospital admission.

Sulfonamide allergies can manifest in several different ways, for example as:
 Sulfonamide drug hypersensitivity syndrome: Symptoms usually start 7 to
14 days after sulfonamide initiation and include fever and a generalized
rash; internal organs may be affected
 Fixed drug eruptions: Symptoms develop within 30 minutes to 8 hours of
taking the drugs and include well-defined, round or oval patches of
redness and skin swelling, sometimes surmounted by a blister
 Type I immediate, IgE-mediated, true allergic response: Hives occur within
30 minutes of drug administration. Anaphylaxis is rare
 Stevens-Johnson Syndrome (SJS) / Toxic Epidermal Necrolysis (TEN):
Serious, potentially fatal skin reaction that usually develops within the first
week of taking the drug. Symptoms include sheets of skin detachment
exposing red, oozing dermis
 Erythema nodosum: Symptoms include red, hot and painful lumps on the
shins or about the knees and ankles, often associated with joint pains or
fever
 Erythema multiforme: Symptoms include the appearance of skin lesions
that look like targets (show three concentric zones of color). May involve
any body site and the lips.

Sulfonamides may also rarely cause changes in the blood such as anemia
(destruction of red blood cells), leukopenia (destruction of white blood cells), and
other hematological side effects.

Renal side effects have been reported with sulfonamide use; more commonly
crystals in the urine (risk is higher in people who are dehydrated) and, rarely,
interstitial nephritis and tubular necrosis.

Note: Sulphites or drugs with a sulfhydryl or sulfate group in their structure (eg,
captopril, morphine sulfate, heparin sulfate) do not need to be avoided by people
with a sulfonamide allergy.

For a complete list of severe side effects, please refer to the individual drug
monographs.

What are the side effects of sulfonamides?


Common side effects reported with sulfonamides include:
 Gastrointestinal effects (such as diarrhea, nausea, stomach
upset, vomiting)
 Candidiasis (overgrowth of the yeast Candida causing conditions such as
thrush) (sulfonamide antibiotics)
 Dizziness
 Fatigue
 Folate deficiency
 Headaches
 Itchy skin
 Rash.

For a complete list of side effects, please refer to the individual drug
monographs.

List of Sulfonamides:
Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Rating

Co-trimoxazole (Pro) 2 reviews 9.0


Generic name: sulfamethoxazole / trimethoprim

Sulfatrim (Pro) 5 reviews 6.7


Generic name: sulfamethoxazole / trimethoprim

Septra (Pro) 17 reviews 6.5


Generic name: sulfamethoxazole / trimethoprim

Septra DS 23 reviews 6.3


Generic name: sulfamethoxazole / trimethoprim

Bactrim (Pro) 417 reviews 5.7


Drug Name Reviews Avg. Rating

Generic name: sulfamethoxazole / trimethoprim

Bactrim DS 304 reviews 5.2


Generic name: sulfamethoxazole / trimethoprim

Sulfatrim Pediatric 1 review 1.0


Generic name: sulfamethoxazole / trimethoprim

Cotrim 0 reviews Add rating


Generic name: sulfamethoxazole / trimethoprim

Gantrisin 0 reviews Add rating


Generic name: sulfisoxazole

Gantrisin Pediatric 0 reviews Add rating


Generic name: sulfisoxazole

Truxazole
Generic name: sulfisoxazole

1. Drug Classes

2. Anti-infectives

3. Glycopeptide Antibiotics
Print Share

Glycopeptide antibiotics
Written by C. Fookes, BPharm on Jul 25, 2018

What are Glycopeptide antibiotics?


Glycopeptide antibiotics are a type of antibiotic that inhibits bacterial cell wall
formation by inhibiting peptidoglycan synthesis. They are used for treating multi-
resistant Staphylococcus aureus (MRSA) infections and enterococcal infections,
which are resistant to beta-lactams and other antibiotics. They are also used in
cases where there is an allergy to beta-lactams.

What are glycopeptide antibiotics used for?


Glycopeptide antibiotics are usually reserved for the treatment of serious
infections caused by MRSA, Streptococcus, or Enterococcus bacteria which are
resistant to beta-lactams and other antibiotics, such as

 Clostridium difficile-associated diarrhea


 Endocarditis
 Enterocolitis
 Pneumonia acquired during a hospital stay or that develops while using a
ventilator
 Severe skin and skin structure infections
 Other serious infections that are not susceptible to other antibiotics.

What are the differences between


glycopeptide antibiotics?
Vancomycin was the first glycopeptide antibiotic approved. The other three
glycopeptides available in the U.S. (dalbavancin, oritavancin, and telavancin)
are structurally related to vancomycin and were developed to improve on
vancomycin’s duration of action and tolerability. However, reports suggest that
one glycopeptide, telavancin, is no more effective than vancomycin and has more
adverse effects.

None are absorbed orally, although vancomycin is effective when given orally for
the treatment of Clostridium difficile-associated diarrhea because this infection is
localized in the gut. Vancomycin and telavancin are given once daily, whereas
dalbavancin is given once weekly or as a single infusion, and oritavancin as a
single infusion.
The need for monitoring in patients receiving vancomycin is controversial, and
the manufacturer does not consider it necessary. There is not considered any
value in monitoring the other glycopeptides.

Generic name Brand name examples

dalbavancin Dalvance

oritavancin Orbactiv

teicoplanin Not approved in the U.S.

telavancin Vibativ

vancomycin oral, vancomycin injection Vancocin HCL pulvules

Are glycopeptide antibiotics safe?


Vancomycin and telavancin may affect kidney function; the risk is greatest in
those older than 65 years. Monitoring of kidney function during and immediately
following treatment may be required. Studies have reported that telavancin
causes more renal adverse effects than vancomycin.

Telavancin can interfere with some clotting tests and can cause prolongation of
the QT interval (the measurement on an ECG that represents electrical
depolarization and repolarization of the ventricles).

Glycopeptides may be ototoxic (toxic to the auditory nerve, cochlear, or


vestibular system of the ear). This may cause transient or permanent hearing
loss. The risk is highest in people given large intravenous doses, with pre-existing
hearing loss, or receiving another ototoxic agent, such as gentamicin.

Rarely, "Red Man Syndrome" has been associated with vancomycin IV and
dalbavancin. Symptoms include flushing of the upper body, shortness of breath,
a skin rash, itching, pain, muscle spasms and low blood pressure. Most
reactions resolve within 20 minutes; however, some may persist for several hours.

Rarely, some people may develop a super-infection due to overgrowth of a


naturally occurring bacterium called Clostridium difficile, following use of any
antibiotic, including glycopeptide antibiotics. Symptoms include severe diarrhea.

For a complete list of severe side effects, please refer to the individual drug
monographs.

What are the side effects of glycopeptide


antibiotics?
Side effects that have been reported with glycopeptide antibiotics include:

 Abdominal pain
 Back pain
 Diarrhea
 Edema
 Flatulence
 Foamy urine
 A headache
 Infusion reactions
 Itchy skin
 Low potassium levels
 Nausea
 Rash
 Taste disturbance
 Urinary tract infection
 Vomiting.

For a complete list of side effects, please refer to the individual drug
monographs.

List of Glycopeptide antibiotics:


Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Vancocin HCl 1 review 10


Generic name: vancomycin

Vancocin (Pro) 1 review 8.0


Generic name: vancomycin

Dalvance (Pro) 1 review 1.0


Generic name: dalbavancin

Orbactiv (Pro) 2 reviews 1.0


Generic name: oritavancin

Firvanq (Pro) 0 reviews Add rating


Generic name: vancomycin

Vancocin HCl Pulvules 0 reviews Add rating


Generic name: vancomycin

Vibativ (Pro)
Generic name: telavancin

Aminoglycosides
What are Aminoglycosides?
Aminoglycosides are a class of antibiotics used mainly in the treatment of aerobic
gram-negative bacilli infections, although they are also effective against other
bacteria including Staphylococci and Mycobacterium tuberculosis. They are
often used in combination with other antibiotics.

Aminoglycosides are thought to work by inhibiting protein synthesis inside


bacteria. Kill rates of bacteria are increased when higher concentrations of
aminoglycosides are present; however, the margin between a safe and a toxic
dose is narrow and monitoring is often needed, although once daily dosing
increases the safety window. Impairment of kidney function and hearing loss are
the most common side effects of aminoglycosides. Aminoglycosides tend to be
used when other less toxic antibiotics are contraindicated or ineffective.

Aminoglycosides are not well absorbed when given by mouth, so need to be


given by injection by healthcare personnel.

List of Aminoglycosides:
Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Tobi (Pro) 0 reviews 9.0


Generic name: tobramycin

Garamycin 0 reviews 8.0


Generic name: gentamicin

Humatin (Pro) 2 reviews 4.0


Generic name: paromomycin

Amikin (Pro) 1 review 2.5


Generic name: amikacin

Amikin Pediatric 0 reviews Add rating


Generic name: amikacin

Arikayce 0 reviews Add rating


Generic name: amikacin liposome

Bethkis (Pro) 0 reviews Add rating


Drug Name Reviews Avg. Ratings

Generic name: tobramycin

Kantrex (Pro) 0 reviews Add rating


Generic name: kanamycin

Kitabis Pak (Pro) 0 reviews Add rating


Generic name: tobramycin

Nebcin 0 reviews Add rating


Generic name: tobramycin

Neo-Fradin (Pro) 0 reviews Add rating


Generic name: neomycin

Neo-Tab 0 reviews Add rating


Generic name: neomycin

TOBI Podhaler (Pro) 0 reviews Add rating


Generic name: tobramycin

Zemdri (Pro)
Generic name: plazomicin

What are Carbapenems?


Carbapenems are a class of beta-lactam antibiotic that are active against many
aerobic and anaerobic gram-positive and gram-negative organisms. Thienamycin
was the first carbapenem to be discovered in 1976. Carbapenems are notable for
their ability to inhibit beta-lactamase enzymes (also called penicillinase) - a type
of enzyme that greatly reduces the activity of antibiotics such as penicillins and
cephamycins. Of all the beta-lactam antibiotics, carbapenems possess the
broadest spectrum of activity and the greatest potency against bacteria. Because
of this, they are often reserved for more severe infections or used as "last-line"
agents.

Carbapenems inhibit bacterial cell wall synthesis by binding to the penicillin-


binding proteins and interfering with cell wall formation.
List of Carbapenems:
Filter by:

View by: Brand | Generic

Drug Name Reviews Avg. Ratings

Doribax (Pro) 1 review 10


Generic name: doripenem

Merrem (Pro) 0 reviews 6.0


Generic name: meropenem

Invanz (Pro) 1 review 1.0


Generic name: ertapenem

Primaxin IM (Pro) 0 reviews Add rating


Generic name: cilastatin / imipenem

Primaxin IV (Pro)
Generic name: cilastatin / imipenem

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