Beruflich Dokumente
Kultur Dokumente
Procaine
Note: This drug and aceclidinum the most common use for
glaucoma
Note:
Note:
Note:
Drug nr. 49
Drug Nr.50
Drug nr.51
Drug nr. 52
Drug nr.53
Drug nr.54
Drug nr 55
Drug nr.56
drug nr.57
Drug nr.59
Drug nr.60
Name of drug : Procainamide
Drug nr.61
Drug nr.62
Drug nr.63
Drug nr.64
Drug nr.65
Drug nr.66
Drug nr.68
Drug nr.69
Drug nr.70
Drug nr.71
Mechanism of action :
Indication : Antihypotensive
Side effects :
Drug nr.72
Functions of cyanocobalamine :
-liver lipotropic.
*drug 90 pentoxyphiline:
side effect:
*drug.93:nikethamide :
*drug.94 :codeine
:ETHIMIZOL.97
Mechanism of action : prevents the decrease of calcium
and creatine phosphate content in the myocardium of rats
exposed to electrical stimulation. The drug was shown to
exert a stimulant action on the heart adenyl cyclase
system. It is suggested that the action mode of ethimizol
on myocardial energy metabolism is connected with an
activation of the adenyl cyclase system followed by the
increased plasma membrane cell permeability by calcium
ions
Indication: reviving newborn infants born in
asphyxia,mixedema,hyperthyreosis
:ACETYLCYSTEINE.98
Mechanism of action : provide cysteine for glutathione
synthesis and possibly to form an adduct directly with the
toxic metabolite of acetaminophen, N-acetyl-p-
benzoquinoneimine. However, these hypothese have not
been tested in vivo, and other mechanisms of action such
as reduction of the quinoneimine might be responsible for
the clinical efficacy of N-acetylcysteine
Indication : sticky, or thick mucus secretions in various
lung problems (eg, chronic emphysema, bronchitis,
asthmatic bronchitis, pneumonia, during
.anesthesia.treatment of paracetamol overdose
Side effect : nausea, vomiting, and diarrhea or
constipation. Rarely, it can cause rashes, fever, headache,
.drowsiness, low blood pressure, and liver problems
:PRENOXDIAZINE.99
Mechanism of action : Prenoxdiazine hydrochloride is an
antitussive or peripherally acting cough suppressant for
nonproductive cough. It acts in the respiratory tract to
.reduce tussal impulses
Indication: Anti-tussive agent, Asthma ,Chronic obstructive
pulmonary disease (COPD) Intestinal Lung disease, Dry
cough, Postoperative Cough
Side effect: allergic reaction , dry mouth, gastric pains,
.constipation, liver and renal disfunction
note: At higher dose levels the patients occasionally *
.experienced slight sedative effect or tiredness
:AMPHEPRAMON.100
Mechanism of action :stimulate release of norepinephrine
from central adrenergic receptors.at higher dosage they
release of dopamine from mesocorticolimbic system and
the nigrodtriatal dopamine system . also it may act on as a
direct agonist on central 5-HT receptors and may inhibit
.monoamine oxidase (MAO)
) weight loss) .indication : obesity
,side effect : agitation ,insomnia,tachycardia,hypertention
Cyproheptadine .101
Mechanism of action :. blocker of serotonin receptors,
cyproheptadine (peritol) on the hypothalamohypophyseal-
adrenal system activity. It has been established in male
rats that the inhibitory, antiserotonin action of peritol on
the indicated system activity depends on the rate and
rhythmicity of the drug administration
Indication: antipruritic, appetite stimulant, antiallergic, and
.for the post-gastrectomy dumping syndrome
Side effect: Drowsiness, dizziness, blurred vision,
.constipation, or dry mouth/nose
.Pirenzepine: 102
Mechanism of action : is a muscarinic receptor antagonist
and binds to the muscarinic acetylcholine receptor. The
muscarinic acetylcholine receptor mediates various
cellular responses, including inhibition of adenylate
cyclase, breakdown of phosphoinositides and modulation
of potassium channels through the action of G protein .
.inhibitor of acid production
Indication : peptic ulcer, gastric ulcer, and duodenal ulcer
Side effect : Dry mouth, blurred vision
note: does not penetrate into CNS thus produce fewer *
. atropine-like side effect
:FAMOTIDINE .103
Mechanism of action : Famotidine is an H2 (histamine)-
receptor antagonist, also known as an H2-blocker.
Histamine is a chemical in some cells of the body that
causes production of acid in the stomach. H2-blockers
inhibit histamine action, and therefore reduce gastric
secretion or the amount of acid produced. Magnesium
hydroxide and calcium carbonate are both antacids that
.function by neutralizing excess gastric acid
Indication : Benign Gastric Ulcer, Duodenal Ulcer,
Gastroesophageal Reflux Disease, Hypersecretory
. Conditions, Heartburn,ulcear healing dyspepsia pain
Side effect : difficulty breathing, swelling of your face,
lips, tongue , diarrhea,constipation,dizziness, depression ,
. sleeplessness,fever,irregular hearbeat
:OMEPRAZOL .104
Mechanism of action : A highly effective inhibitor of gastric
acid secretion used in the therapy of stomach ulcers and
Zollinger-Ellison syndrome. Omeprazole belongs to a class
of antisecretory compounds, the substituted
benzimidazoles, that suppress gastric acid secretion by
specific inhibition of the H+/K+ ATPase enzyme system at
the secretory surface of the gastric parietal cell
Indication : treat reflux esophagitis , promotes peptic
ulcer healing
Side effect : constipation,chest pain , headache,gas rash ,
.drowsiness
:FESTAL :106
Mechanism of action : Festal works by stimulating better
digestion of food and promoting
better absorption of nutrients in the body. This enzymic
preparation aids in the relief of gastro intestinal disorder
by acting directly in the bodys digestive organ
Festal compensates the insufficient amount of digestive
enzymes in the body essential for the digestion of food
and for complete absorption of nutrients. Festal improves
the functions of the pancreatic gland for better secretion
function
:METOCLOPRAMIDE .108
Mechanism of action : 1) inhibition of presynaptic and
postsynaptic D2 receptors, 2)stimulation of presynaptic
excitatory 5-HT4 receptors and 3)antagonism of
presynaptic inhibition of muscarinic receptors (Figure 2A).
This promotes release of acetylcholine, which in turn leads
to increased lower esophageal sphincter (LES) and gastric
tone, increased intragastric pressure, improved
antroduodenal coordination and accelerated gastric
.emptying
Indication : reflux esophagitis , promote peptic uler
healing
Side effect : diarrhea,less frequently may cause
involuntary movement of limbs ,
. restlessness,drowsiness,muscle tremor,spasms
:ONDANSETRON .109
Mechanism of action : Ondansetron is a selective
serotonin 5-HT3 receptor antagonist. The antiemetic
activity of the drug is brought about through the inhibition
of 5-HT3 receptors present both centrally (medullary
chemoreceptor zone) and peripherally (GI tract). This
inhibition of 5-HT3 receptors in turn inhibits the visceral
afferent stimulation of the vomiting center, likely indirectly
at the level of the area postrema, as well as through direct
inhibition of serotonin activity within the area postrema
.and the chemoreceptor trigger zone
Indication : For the prevention of nausea and
vomiting associated with emetogenic cancer
chemotherapy, postoperation, and radiation. Also used for
. the treatment of postoperative nausea and vomiting
Side effect : Confusion, dizziness, fast heartbeat ,
.fever, headache, shortness of breath, weakness
:COLOSAS .110
mechanism of action :hepatoprotective action. :
Restores and maintains normal function of hepatocytes,
warns chronization process, restores the flow of bile, and
normalizes the immune system, has anti-inflammatory,
diuretic effect, enhances the motility of the intestine. Due
to the presence of vitamin C and other bioactive natural
products, has a tonic effect, increases immunity.(unclear
(mechanism ..in the book page 372)
Indication: avitaminosis,anemia,hypovitaminosis ,
low blood pressure caused by cardiac and coronary
insufficiency,gall bladder inflammation, hepatitis ,
Cholecystitis
,Side effect : joint pain, gastric upset
: SILIBINIne.111
Mechanism of action : silibinin has hepatoprotective
(antihepatotoxic) properties that protect liver cells against
toxins.[2][3] Silibinin has also demonstrated in vitro anti-
cancer effects against human prostate adenocarcinoma
cells, estrogen-dependent and -independent human breast
carcinoma cells, human ectocervical carcinoma cells,
human colon cancer cells, and both small and nonsmall
human lung carcinoma cells
Indication : severe intoxications with hepatotoxic
substances, such as death cap (Amanita phalloides)
poisoning There is also clinical evidence for the use of
silibinin as supportive element in alcoholic and child grade
'A' liver cirrhosis
Side effect : laxative effect , nausea, diarrhea,
indigestion, intestinal gas, bloating, fullness or pain, and
loss of appetite
:ESENTIALE.112
: Mechanism of action
. : Indication
:Side effect
DROTAVERINE .113
Mechanism of action : Drotaverine inhibits
phosphodiesterases hydrolysing cAMP, thereby increasing
cAMP concentration, decreasing Ca uptake of the cells and
changing the distribution of calcium among the cells. It
may also have minor allosteric calcium channel blocking
properties
Indication: Used in the treatment of functional bowel
.disorders and alleviating pain in renal colic
.Side effect : nausea, vomiting and dry mouth
:Indomethacin .114
Mechanism of action : prostaglandin G/H synthase (also
known as cyclooxygenase or COX) inhibitor that acts on
both prostaglandin G/H synthase 1 and 2 (COX-1 and -2).
Prostaglandin G/H synthase catalyzes the conversion of
arachidonic acid to a number of prostaglandins involved in
fever, pain, swelling, inflammation, and platelet
aggregation. Indomethacin antagonizes COX by binding to
the upper portion of the active site, preventing its
substrate, arachidonic acid, from entering the active site.
Indomethacin, unlike other NSAIDs, also inhibits
phospholipase A2, the enzyme responsible for releasing
arachidonic acid from phospholipids. Indomethacin is more
selective for COX-1 than COX-2, which accounts for its
increased adverse gastric effects relative to other NSAIDs.
COX-1 is required for maintaining the protective gastric
mucosal layer. The analgesic, antipyretic and anti-
inflammatory effects of indomethacin occur as a result of
decreased prostaglandin synthesis. Its antipyretic effects
may be due to action on the hypothalamus, resulting in an
increased peripheral blood flow, vasodilation, and
.subsequent heat dissipation
Indication : severe rheumatoid arthritis including acute
flares of chronic disease, ankylosing spondylitis,
osteoarthritis, acute painful shoulder (bursitis and/or
.tendinitis) and acute gouty arthritis
Side effect : heart attack, stroke, skin changes (paleness)
weight gain, swelling, shortness of breath, tachycardia,
unusual bleeding (including GI bleeding), jaundice,
stomach pain, and pain with urination, bloody urine, blurry
.vision, and back pain
note: Patients with asthma that are aspirin-sensitive *
.should avoid use of this drug
: PIROXICAM.116
Mechanism of action : The antiinflammatory effect of
Piroxicam may result from the reversible inhibition of
cyclooxygenase, causing the peripheral inhibition of
prostaglandin synthesis. The prostaglandins are produced
by an enzyme called Cox-1. Piroxicam blocks the Cox-1
enzyme, resulting into the disruption of production of
prostaglandins. Piroxicam also inhibits the migration of
leukocytes into sites of inflammation and prevents the
formation of thromboxane A2, an aggregating agent, by
.the platelets
.Indication : osteoarthritis and rheumatoid arthritis
Side effect : Upset stomach, nausea, dizziness,
.drowsiness, or headache
:IBUPROFEN.117
Mechanism of action : Ibuprofen is a non-selective
inhibitor of cyclooxygenase, an enzyme invovled in
prostaglandin synthesis in the arachidonic acid pathway
Indication : rheumatoid arthritis, osteoarthritis, acute gout
. Side effect : nausea,vomiting , abdominal pain
note: Ibuprofen, a propionic acid derivative, is a *
prototypical nonsteroidal anti-inflammatory agent (NSAIA)
.with analgesic and antipyretic properties
:NIMESULID.118
mechanism of action : is a relatively COX-2 selective,
non-steroidal anti-inflammatory drug (NSAID) with
.analgesic and antipyretic properties
Indication : acute pain, the symptomatic treatment of
.osteoarthritis and primary dysmenorrhoea in adolescents
Side effect : Abdominal discomfort, heartburn, abdominal
cramps, nausea, vomiting and diarrhea. Headache,
dizziness and drowsiness, Blood in urine, decrease in
.urination and kidney failure
:LEVAMIZOL.119
Mechanism of action : an antiparasitic agent appears to be
tied to its agnositic activity towards the L-subtype nicotinic
acetylcholine receptors in nematode muscles. This
agonistic action reduces the capacity of the males to
control their reproductive muscles and limits their ability
to copulate. The mechanism of action of Levamisole as an
anticancer drug in combination with fluorouracil is
unknown. The effects of levamisole on the immune system
are complex. The drug appears to restore depressed
immune function rather than to stimulate response to
above-normal levels. Levamisole can stimulate formation
of antibodies to various antigens, enhance T-cell
responses by stimulating T-cell activation and
proliferation, potentiate monocyte and macrophage
functions including phagocytosis and chemotaxis, and
.increase neutrophil mobility, adherence, and chemotaxis
Indication : anthelminthic and immunomodulator,
prescribed for cancer treatment and also used for
roundworm infection. It interferes with the growth of
cancer cells and slows their growth and spread in the
.body. It is used in the treatment of colon cancer
Side effect : Memory loss, loss of consciousness, fatigue,
speech disturbances, Muscle weakness, difficulty in
breathing , welling of lips, tongue, face, fever and chills
:DIFEMIYDRAMINE.120
Mechanism of action : A histamine H1 antagonist used as
an antiemetic, antitussive, for dermatoses and pruritus,
for hypersensitivity reactions, as a hypnotic, an
antiparkinson, and as an ingredient in common cold
preparations. It has some undesired antimuscarinic and
.sedative effects
Indication : nausea and vomiting, motion sickness and
,insect bite
Side effect : edation, tiredness, sleepiness, dizziness,
disturbed coordination, constipation, dry
mouth/nose/throat, difficulty urinating, and upset
.stomach
Drug 121 : name of drug : loratidine :*
-Mechanism of action : antihistamines block tissue
receptors sensitive to histamine (block H1-receptors).
-indications : allergic damage to the skin and mucosal
membrane :urticaria ,angioneurotic edema, hay fever,
rhinitis, and conjunctivitis .
-side effects: fast or uneven heart rate, jaundice
(yellowing of your skin or eyes); or seizures (convulsions)
headache, nervousness; feeling tired or drowsy, stomach
pain, diarrhea, dry mouth, sore throat hoarseness ,eye
redness, blurred vision; nosebleed; or skin rash ,slight
sedative effect, tolerance.
-notes : in case of hepatic and renal disturbances,
antihistamines should be used with caution. It's effect
lasts 24 hours.
Drug 122 : name of drug : clemastine :*
-mechanism of action : : antihistamines block tissue
receptors sensitive to histamine (block H1-receptors).
-indications : allergic damage to the skin and mucosal
membrane :urticaria ,angioneurotic edema, hay fever,
rhinitis, and conjunctivitis .
-side effects : Dizziness; drowsiness; dry mouth, throat,
and nose; excitability; thickening of mucus in nose or
throat. Other severe side effects : Severe allergic reactions
(rash; hives; difficulty breathing; tightness in the chest;
swelling of the mouth, face, lips, or tongue); convulsions;
fast heartbeat or pounding in the chest; decreased
alertness; hallucinations; tremor; wheezing. slight sedative
effect.
-notes: : in case of hepatic and renal disturbances,
antihistamines should be used with caution. It's effect
lasts 8-12 hours.it is a derivative of ethanolamine.
Drug 123 : name of drug : chloropyramine : *
-mechanism of action : : antihistamines block tissue
receptors sensitive to histamine (block H1-receptors).
-indications : allergic damage to the skin and mucosal
membrane :urticaria ,angioneurotic edema, hay fever,
rhinitis, and conjunctivitis .
-side effects : Dry mouth, Drowsiness, Dizziness ,Nausea
and vomiting, Restlessness or moodiness (in some
children), Trouble urinating or not being able to urinate,
Blurred vision , Confusion.
-notes : in case of hepatic and renal disturbances,
antihistamines should be used with caution. It's effect
lasts 4-6 hours.it is a derivative of ethylendiamines .it has
inhibitory influence on th CNS (due to the blockage of
central H1-receptors). This is manifested by sedative and
hypnotic effects.
*Drug 124 : name of drug : oxytocin :
-mechanism of action : increasing the contractile activity
of the myometrium by changing calcium concentrations
in the uterine muscle cells .at the same time the tone of
the myometrium also increases (especially if oxytocin is
used in high doses).
-indications :in order to induce and stimulate labor, or in
treatment of hemorrhage and atonia of the uterus during
the puerperium (period after labor).
-side effects : Nausea; vomiting; more intense or abrupt
contractions of the uterus.
More severe side effects : Severe allergic reactions (rash;
hives; itching; difficulty breathing; tightness in the chest;
swelling of the mouth, face, lips, or tongue); blood clotting
problems; changes in heart rate; heavy or continued
bleeding after childbirth; irregular heartbeat; pooling of
blood in the pelvis; ruptured uterus.
-notes :the pregnant uterus is more sensitive to oxytocin
than the non-pregnant one.the sensitivity of the uterus to
the oxytocin increases as the pregnancy advances,
reaching its maximum during labor and for several days
afterwards. oxytocin can also contribute to milk secretion
(due to increased release of prolactin from anterior lobe of
the pituitary ) and milk let-down (due to the excitation of
myoepithelial elements of the mammary gland). Oxytocin
is administered intravenously together with glucose
solution. The doses are measured in activity units (AU).
*Drug 125: name of drug : levothyroxine :
-mechanism of action : Levothyroxine is a replacement for
a hormone normally produced by your thyroid gland to
regulate the body's energy and metabolism.
Mechanism of action
Vitamin E exhibit antioxidant activity
Vitamin E's anti-atherogenic activity involves the inhibition
of the oxidation of LDL and the accumulation of LDL in the
arterial wall. It also appears to reduce LDL-induced
apoptosis in human endothelial cells.
In addition, vitamin E inhibits protein kinase C activity.
PKC plays a role in smooth muscle cell proliferation, and,
thus, the inhibition of PKC results in inhibition of smooth
muscle cell proliferation, which is involved in
atherogenesis.
Vitamin E's antithrombotic and anticoagulant vitamin E
upregulates the expression of cytosolic phospholipase A2
and cyclooxygenase (COX)-1 which in turn enhances the
release of prostacyclin. Prostacyclin is a vasodilating factor
and inhibitor of platelet aggregation and platelet release.
Indication
cardiovascular disease , some forms of cancer ,immune-
enhancing effects, asthma , rheumatoid arthritis,
neurological diseases Alzheimer's, eye disorders including
cataracts, diabetes , premenstrual syndrome, protect skin
from ultraviolet irradiation male fertility.
Side effect
Blurred vision ,diarrhea ,dizziness ,headache nausea or
stomach cramps, unusual tiredness or weakness
Name of Drug :146. Hialuronidaze
Mechanism of action
Hyaluronidase is a spreading or diffusing substance. It
increase the permeability of connective tissue through the
hydrolysis of hyaluronic acid. Hyaluronidase hydrolyzes
hyaluronic acid by splitting the glucosaminidic bond
between C1 of the glucosamine moiety and C4 of
glucuronic acid. This temporarily decreases the viscosity
of the cellular cement and increases diffusion of injected
fluids or of localized transudates or exudates, thus
facilitating their absorption.
Indication
For increase of absorption and distribution of other
injected drugs and for rehydration
Side effect
Cough ,difficulty swallowing ,dizziness ,fast heartbeat
,swelling on the face, eyelids, lips, tongue, throat, hands,
legs, feet, or sex organs, redness of the skin, skin rash
tightness in the chest ,unusual tiredness or weakness
Mechanism of action
The exact mechanism of action is unknown. Nitrofurazone
inhibits several bacterial enzymes, especially those
involved in the aerobic and anaerobic degradation of
glucose and pyruvate. This activity is believed also to
affect pyruvate dehydrogenase, citrate synthetase, malate
dehydrogenase, glutathione reductase, and pyruvate
decarboxylase.
Indication
bacterial skin infections ,pyodermas, infected dermatoses
and infections of cuts, wounds, burns and ulcers ,
trypanosomiasis
Side effect
Cough ,difficulty swallowing ,dizziness ,fast heartbeat
,swelling on the face, eyelids, lips, tongue, throat, hands,
legs, feet, or sex organs, redness of the skin, skin rash
tightness in the chest.
Name of Drug :148. Chlorhexidine
Mechanism of action
Chlorhexidine's antimicrobial effects are associated with
the attractions between chlorhexidine (cation) and
negatively charged bacterial cells. After chlorhexidine is
absorpted into the organism's cell wall, it disrupts the
integrity of the cell membrane and causes the leakage of
intracellular components of the organisms.
Indication
periodontitis, used as an adjunct to scaling and root
planing procedures. Also for prevention of dental caries,
oropharyngeal decontamination in critically ill patients,
hand hygiene in health-care personnel, general skin
cleanser, and catheter used also as mouthwash to prevent
oral plaque
Side effect
Blistering, burning, itching, peeling, skin rash, redness,
swelling, or other signs of irritation on the skin,swelling of
the face, hands, or feet ,trouble breathing,
Hypersensitivity.
Name of Drug : 149.potassium permanganate
Mechanism of action
a strong oxidizing agent used in solution as an antiseptic
and deodorizing application for malodorous lesions, and
formerly as a gastric lavage in poisoning from morphine,
strychnine, aconite, and picrotoxin;
Indication
Bromhidrosis, Dermatophytic infection, fungal infection,
hyperhidrosis infected genital or oral lesion
Side effect
Ulceration, Corrosive burns, Nausea, Vomiting, Cyanosis,
Methemoglobinemia, GI ulceration, Oral ulceration,
Metabolic acidosis, Cardiopulmonary arrest,
Hypermangnesemia, Corrosive pleurisy, Pericarditis.
Note
Mechanism of action
The preparation has high antimicrobial activity especially
it is very effective against staphylococcus and
streptococcus, But it is not very effective against Aureus
streptococcus, if there are organic substances blood
serum, pus. It stimulates wound granulation.
Indication
post_operative , post_traumatic scars, bruises, pyoderma,
burns, bedsores, blepharitis.
Side effect
Skin rash, allergy , redness
Mechanism of action
By binding to specific penicillin-binding proteins (PBPs)
located inside the bacterial cell wall, penicillin G inhibits
the third and last stage of bacterial cell wall synthesis. Cell
lysis is then mediated by bacterial cell wall autolytic
enzymes such as autolysins; it is possible that penicillin G
interferes with an autolysin inhibitor.
Indication
severe infections, septicemia, meningitis, pericarditis,
endocarditis and severe pneumonia.
Side effect
Neurological disorders, Neutropenia can occur if high
doses are administered consistently for over 2 weeks.
Mechanism of action
By binding to specific penicillin-binding proteins (PBPs)
located inside the bacterial cell wall, Ampicillin inhibits the
third and last stage of bacterial cell wall synthesis. Cell
lysis is then mediated by bacterial cell wall autolytic
enzymes such as autolysins; it is possible that Ampicillin
interferes with an autolysin inhibitor.
Indication
infection Respiratory, GI, UTI and meningitis due to E. coli,
P. mirabilis, enterococci, Shigella, Salmonella N.
gononhoeae, H. influenzae, staphylococci, streptococci
including streptoc
Side effect
diarrhea, nausea, rash Hypersensitivityt hrombocytopenia,
thrombocytopenic headache, and dizziness
Mechanism of action
Amoxicillin is a semisynthetic antibiotic with in vitro
bactericidal activity against Gram-positive and Gram-
negative bacteria. Amoxicillin is, however, susceptible to
degradation by beta-lactamases, and therefore, the
spectrum of activity does not include organisms which
produce these enzymes. Clavulanic acid is a beta-lactam,
structurally related to the penicillins, which possesses the
ability to inactivate some beta-lactamase enzymes
commonly found in microorganisms resistant to penicillins
and cephalosporins. In particular, it has good activity
against the clinically important plasmid-mediated beta-
lactamases frequently responsible for transferred drug
resistance.
Indication
infections of the ear, nose, and throat, the genitourinary
tract, the skin, lower respiratory tract acute uncomplicated
gonorrhea
Side effect
Itching of the vagina or genital area pain during sexual
intercourse
redness of the skin ,skin rash ,Bloody or cloudy urine
,fever , decreased urination seizures ,swelling of the feet
or lower legs
Name of Drug : 154.Imipenem
Mechanism of action
Imipenem acts as an antimicrobial through the inhibition
of cell wall synthesis of various gram-positive and gram-
negative bacteria. This inhibition of cell wall synthesis in
gram-negative bateria is attained by binding to pencillin
binding proteins (PBPs). This preferential binding to PBP-2
and PBP-1b results in the direct conversion of the
individual cell to a spheroblast, which leads to rapid cell
lysis and death without filament formation.
Indication
For the treatment of bacterial infections caused by
susceptible bacteria.
Side effect
Confusion seizures dizziness ain at place of injection ,skin
rash, hives, itching, fever, or wheezing tremors
Mechanism of action
The bactericidal action of aztreonam results from the
inhibition of bacterial cell wall synthesis due to a high
affinity of aztreonam for penicillin binding protein 3
(PBP3). By binding to PBP3, aztreonam inhibits the third
and last stage of bacterial cell wall synthesis. Cell lysis is
then mediated by bacterial cell wall autolytic enzymes
such as autolysins. It is possible that aztreonam interferes
with an autolysin inhibitor.
Indication
urinary tract infections, lower respiratory tract infections,
septicemia, skin and skin-structure infections, intra-
abdominal infections, and gynecologic infections.
Side effect
Chest discomfort ,cough ,difficulty with breathing or
troubled breathing ,fever, Noisy breathing, shortness of
breath ,tightness chest
Mechanism of action
Erythromycin acts by penetrating the bacterial cell
membrane and reversibly binding to the 50 S subunit of
bacterial ribosomes or near the P or donor site so that
binding of tRNA to the donor site is blocked. Translocation
of peptides from the A or acceptor site to the P or
donor site is prevented, and subsequent protein synthesis
is inhibited. Erythromycin is effective only against actively
dividing organisms. The exact mechanism by which
erythmromycin reduces lesions of acne vulgaris is not fully
known: however, the effect appears to be due in part to
the antibacterial activity of the drug.
Indication
respiratory tract infections (upper and lower), pertussis
(whooping cough), as adjunct to antitoxin in infections due
to Corynebacterium diphtheriae, intestinal amebiasis
acute pelvic inflammatory disease, skin and soft tissue
infections, primary syphilis, urethritis ,Legionnaires'
disease
Side effect
diarrhea, nausea, stomach cramps, and vomiting.
Mechanism of action
Clarithromycin is first metabolized to 14-OH
clarithromycin, which is active and works synergistically
with its parent compound. Like other macrolides, it then
penetrates bacteria cell wall and reversibly binds to
domain V of the 23S ribosomal RNA of the 50S subunit of
the bacterial ribosome, blocking translocation of
aminoacyl transfer-RNA and polypeptide synthesis.
Clarithromycin also inhibits the hepatic microsomal
CYP3A4 isoenzyme and P-glycoprotein, an energy-
dependent drug efflux pump.
Indication
acute otitis ,patients with a history of type I penicillin
hypersensitivity, pharyngitis and tonsillitis ,respiratory
tract infections including acute maxillary sinusitis, acute
bacterial exacerbations of chronic bronchitis, community-
acquired pneuomia, Legionnaires' disease, and pertussis.
skin or skin structure infections, helicobacter pylori
infection, duodenal ulcer disease, bartonella infections,
early Lyme disease, and encephalitis, endocarditis.
Side effect
Symptoms of toxicity include diarrhea, nausea, abnormal
taste, dyspepsia, and abdominal discomfort, Transient
hearing loss with high doses has been observed,
Pseudomembraneous colitis has been reported with
clarithromycin use, Allergic reactions ranging from
urticaria and mild skin eruptions to rare cases of
anaphylaxis and Stevens-Johnson syndrome, hepatic
dysfunctions, tooth decolouration , cardiovascular defects
- QT prolongation.
Mechanism of action
Azithromycin binds to the 50S subunit of the 70S bacterial
ribosomes, and therefore inhibits RNA-dependent protein
synthesis in bacterial cells.
Indication
For the treatment of patients with mild to moderate
infections caused by susceptible strains of the designated
microorganisms in the specific conditions: H. influenzae,
M. catarrhalis, S. pneumoniae, C. pneumoniae, M.
pneumoniae, S. pyogenes, S. aureus, S. agal
Side effect
oedema and cholestatic jaundice, Diarrhea, loose stools,
Blistering, crusting, irritation, itching, skin dry, or scaly
skin, fever, swelling.
Name of Drug :159. Lincomycin
Mechanism of action:
Lincomycin inhibits protein synthesis in susceptible
bacteria by binding to the 50 S subunits of bacterial
ribosomes and preventing peptide bond formation upon
transcription. It is usually considered bacteriostatic but
may be bactericidal in high concentrations or when used
against highly susceptible organisms.
Indication:
Endocarditis, septicemia, bone infection,Skin infection,
lower respiratory infection.
Side effect:
Diarrhea ,Nausea Vomiting, Stomach pain
,Hypersensitivity,Jaundice Erythema multiforme,
exfoliative and vesiculobullous dermatitis, rash, Stevens-
Johnson syndrome, urticarial, Cardiopulmonary arrest,
Azotemia; oliguria; proteinuria; vaginitis, Agranulocytosis;
aplastic anemia; leukopenia; neutropenia; pancytopenia;
thrombocytopenic purpura.
Mechanism of action:
Cephalexin, like the penicillins, is a beta-lactam antibiotic.
By binding to specific penicillin-binding proteins located
inside the bacterial cell wall it inhibits the third and last
stage of bacterial cell wall synthesis that cause bacterial
cell wall autolytic enzymes such as autolysins it is possible
that cephalexin interferes with an autolysin inhibitor.
Indication:
Respiratory tract infection, Skin infections, Bone
infections, Genitourinary tract infections, Acute prostatitis
Side effect:
Diarrhea, Dizziness, Fever, General tiredness and
weakness, Headache, itching, Joint or muscle pain
Mechanism of action:
Cefuroxime like the penicillins is a beta-lactam antibiotic
its binding to specific penicillin-binding proteins located
inside the bacterial cell wall and its inhibit the third and
last stage of bacterial cell wall synthesis that lead to
bacterial cell wall autolytic enzymes such as autolysins it
is possible that cefuroxime interferes with an autolysin
inhibitor
Indication:
Bronchitis, Sinusitis, Tonsillitis, Ear infections, Skin
infections Gonorrhea, Urinary tract infections
Side effect:
Allergic reactions ,Skin rash, Nasal congestion, Cough, Dry
throat, Eye irritation, Anaphylactic shock, Cerebral
irritation
Mechanism of action:
The bactericidal activity of cefotaxime results from the
inhibition of cell wall synthesis via affinity for penicillin-
binding proteins
Indication:
Gonorrhea, Meningitis, Severe infections , Infections of the
kidney Urinary system, Prevent infection after surgery.
Side effect:
Nausea Vomiting, Epigastria distress, Diarrhea,
Convulsions, Dizziness, Fast heartbeat, Fever, Difficulty
with breathing swallowing
Indication:
bacterial neonatal sepsis, bacterial septicemia, serious
bacterial infections of the central nervous system
meningitis, urinary tract, respiratory tract, gastrointestinal
tract including peritonitis, skin, bone and soft tissue
including burns.
Side effect:
Nephrotoxicity, Drug accumulation in the endolymph and
perilymph of the inner ear causes irreversible damage to
hair cells of the cochlea or summit of ampullar cristae in
the vestibular complex,Toxicity may lead to retrograde
degeneration of the 8th cranial (vestibulocochlear) nerve.
Vestibular toxicity may cause vertigo, nausea, vomiting,
dizziness and loss of balance
Mechanism of action:
Chloramphenicol is lipid-soluble allowing it to diffuse
through the bacterial cell membrane its reversibly binds to
the L16 protein of the 50S subunit of bacterial ribosomes
where transfer of amino acids to growing peptide chains is
prevented thus inhibiting peptide bond formation and
subsequent protein synthesis.
Indication:
cholera ,eye drops or ointment to treat bacterial
conjunctivitis
Side effect:
abdominal distension with or without emesis, cyanosis
vasomotor collapse, irregular respiration Note:
Indication:
typhus fever ,Infections like Lyme disease ,Upper
respiratory infections S. pneumonia, H. influenza,Acne
,People who are allergic to penicillin
Side effect:
Increased sensitivity of skin to sunlight, Headache, Nausea
Vomiting, Yellow skin, Visual changes, Loss of appetite,
Abdominal pain
Indication:
Respiratory tract infections ,Malaria ,bacterial infections
plague tetanus,Campylobacter fetus
Side effect:
Anorexia, Nausea, Diarrhea, Dysphagia, Inflammatory
lesions Dermatitis, Hypersensitivity , Urticarial,
Anaphylaxis, Pericarditis Intracranial hypertension,
Thrombocytopenia, Neutropenia, Eosinophilia.
Note:
Side effect:
Dizziness, Drowsiness, Fever, Headache, Pain in lower
back
Note: parenteral
Indication:
Skin infection, endocarditis, bone infection, lung infection,
septicemia, osteomyelitis, Thrombophlebitis
Side effect:
Bladder pain ,Decreassed urine, Painful urination, Dry
mouth
Fever, Irregular heartbeat, Muscle pain , Loss of appetite,
Mood change, Nausea vomiting, Rapid weight gain ,
Shortness of breath