- Alimentary System
- Cardiovascular & Hematopoietic System
- Respiratory System
- Neuro-Muscular System
- Hormones
- Contraceptive Agents
- Antibiotics
- Other Chemotherapeutics
- Genito-Urinary System
- Metabolism (Anti-Cholesterol/Osteoporosis)
- Eye, Ear, Mouth & Throat
- Dermatologicals
- Anaesthetics – Local & General
- Allergy & Immune System
- Antidotes & Detoxifying Agents
- Intravenous & Other Sterile Solutions
- Miscellaneous
Cardiovascular & Hematopoietic System
a) Cardiac Drugs
Amiodarone HCI
treatment of severe rhythm disorders eg atrial or nodal
rhythm disorders, ventricular rhythm disorders, those associated
w/ Wolff-Parkinson-White syndrome. Amp Where a rapid response
is required or where oral administration is not possible.
AV or SA block, sinus bradycardia, sick sinus syndrome
except when used in conjunction w/ a pacemaker; history
of thyroid dysfunction; iodine intolerance, severe arterial
hypotension, CV collapse, acute cardiac insufficiency. Combined
therapy w/ drugs which may induce torrsades de pointes.
Pregnancy, lactation.
Hypotension, severe resp failure, decompensated cardiomyopathy
or severe heart failure.
Reversible corneal microdeposits; coloured halos; hyper
or hypothyroidism. Rarely, photosensitization & pigmentation,
resersible diffuse interstitial pneumopathy or peripheral
neuropathy.
Antiarrthythmics, ß-blockers, stimulating laxatives,
diuretics inducing hypokalemia, systemic corticosteroids,
tetracosactide, amphotericin B, digitalis, anticoagulants,
phenytoin, general anesth, cyclosporine.
Dobutamine HCI
Positive inotropic treatment of forward & backward
failure in acutely decompensated chronic heart failure.
Mechanical impedence of ventricular filling &/or
emptying eg in pericardial tamponade, constrictive pericarditis,
hypertrophic obstructive cardiomyopathy & severe aortic
stenosis. Severe hypovolaemic states. Concomitant administration
of MAOIs.
Tolerance phenomena may develop w/ continuous administration
for >72 hr, thereby necessitating an increase in dosage.
Deterioration of clinical symptoms may occur in patients
w/ severe CHD. Caution in ischaemic heart disease. Pregnancy
& lactation.
Tachycardia, hypertension, hypotension, inducement or
enhancement of ventricular arrhythmias, mild vasoconstriction.
Headache, nausea, chest pains, palpitations & shortness
of breath. Occasionally skin rash, fever, oesinophilia &
bronchospasm. Lowering of serum K levels.
ß-blockers, venously acting vasodilators, ACE
inhibitors, dopamine.
Amrinone lactate
Short-term management of CHF.
Severe aortic or pulmonary valvular disease in lieu
of surgical relief of the obstruction.
Monitor BP & heart rate, fluid & electrolytes
& renal function.
GI upsets; arrhythmia, hypotension; hypersensitivity;
thrombocytopenia, hepatotoxicity.
Excessive hypotension w/ disopyramide.
Digoxin.
Whenever digitalis therapy is required for the treatment
of CHF, atrial fibrillation; flutter & supraventricular
tachycardia.
Supraventricular dysrhythmias caused by Wolff-Parkinson-white
syndrome; hypersensitivity to cardiac glycosides.
Acute myocarditis w/ failure; renal failure (decrease
dose & monitor closely); hypokalaemia;hypercalcaemia;
hypomagnesaemia; hypothyroidism; w/hold Lanoxin for 24-48hrs
before electroconversion.
Nausea, vomiting, anorexia, diarrhoea, abdominal pains,
salivation, sweating; headache, facial pain, malaise, fatigue,
drowsiness, depression, disorientation, mental confusion,
delirium, hallucination, visual disturbance. Ventricular
premature contractions, atrial or ventricular arrhythmias
& conduction effects. Hypokalaemia.
Plasma conc increased by quinidine, verapamil, nifedipine,
amiodarone. Hypokalemia may be associated w/ diuretics,
lithium, carbenoxolone, corticosteroids. Antacids, neomycin
may reduce serum level of digoxin.
b) Anti-Anginal Drugs
Isosorbide mononitrate.
Long-term treatment of CHD & CHF.
Acute MI w/ low filling pressures, acture circulatory
failure, very low BP.
1st trimester of pregnancy. May impair ability to drive
or operate machinery.
Nitrate headache. Manifestations of collapse may arise
after the 1st dose in patients w/ circulatory lability.
Effects may be enhanced by alcohol & antihypertensives.
Isosorbide-5-mononitrate.
prophylactic treatment of angina pectoris.
Initiate at 30 mg once daily for 1st 2-4 days. Increase
to 60 mg once daily thereafter. Max: 120mg once daily. Do
not administer bd.
Cardiogenic shock, head trauma, cerebral hemorrhage,
severe hypotension, severe hypovolemia.
Severe cerebral arteriosclerosis, hypotension.
Headache, dizziness, nausea.
Hypotensive effects enhanced by alcohol, antihypertensives,
tricyclic antidepressants, narcotics.
Isosorbide dinitrate.
Prophylaxis of ischemic heart pain associated w/ coronary
insufficiency.
5-30 mg bd-qds.
Hypersensitivity.
Tolerance & cross-tolerance to other nitrates &
nitrites may occur. Pregnancy, lactation, childn. Patients
prone to or affected by hypotension or vol depletion; severe
hypotensive response; paradoxical bradycardia, increased
angina may accompany nitrate induced hypotension, hypertrophic
cardiomyopathy.
Flushing, vascular headache, cerebral ischemia associated
w/ postural hypotension, nausea, vomiting, weakness, restlessness,
pallor, perspiration & collapse; drug rash &/or
exfoliative dermatitis.
Increased hypotensive effects w/ alcohol, ß-adrenergic
blockers, phenothiazines, sildenafil.
Trimetazidine diHCI.
Treatment of angina pectoris. Adjuvant treatment of vertigo;
tinnitus; decline in visual acuity & visual field disturbances
of vascular origin.
Concomitant administration w/ MAOIs.
Pregnancy esp 1st trimester.
Rare cases of GI disorders.
c) ACE-Inhibitors/ other Antihypertensives
Quinapril.
Hypertension, CHF
Renal insufficiency, severe CHF.
Headache, dizziness, rhinitis, cough, upper resp tract
infection, fatigue, nausea, vomiting, dyspepsia & paresthesia.
May reduce the absorption oftetracyclines. Serum K monitoring
when used w/ K-sparing diuretics, K supplements, or K-containing
salt substitutes.
Methyldopa.
Hypertension.
Active hepatic disease.
History of liver disease. +ve Coombs’ test. Phaeochromocytoma.
Discontinuetherapy if unexplained persistent fever, liver
dysfunction or jaundice occur. Crosses placental barrier
& appears in breast milk.
Sedation (usually transient), headache, asthenia, oedema.
Rarely, drug fever, CNS, CVS, hepatic effects, endocrine
& GI disturbances, allergic & dermatologic reactions.
Bone marrow depression (usually reversible), haemolytic
anemia (stop drug), jaundice, involuntary choreoathetotic
movements.
Antihypertensive drugs, lithium, MAOIs.
Irbesartan.
essential hypertension.
pregnancy, lactation.
Increased risk of severe hypotension in patients w/
rena; artery stenosis. Periodic monitoring of K & serum
creation in patients w/ renal impairment. Monitoring of
serum K in patients suffering from heart failure. Patients
w/ recent kidney transplantation, primary aldosteronism,
aortic or mitral stenosis, obstructive hypertrophic cardiomyopathy,
ischaemic cardiopathy or ischaemic cardiovascular disease.
Flushing
Increased hypotensive effect w/ other hypotensive agents.
K supplements & K-sparing diuretics may lead to increases
in serum K. Monitor for possible increase in serum concentration
of lithium.
Captopril.
Hypertension, Heart failure, MI, Diabetic nephropathy
Pregnancy. Hypersensitivity.
renal impairment, collagen vascular cisease, immunosuppressant
therapy (neutropenia); bilateral renal artery stenosis;
aortic steenosis.
Rash, pruritus, flushing; angioedema; loss of taste
perception; stomatitis; GI irritation & abdominal pain;
leucopenia; cough.
May increase serum K w/ K-sparing diuretics. Hypotensive
effects enhanced by diuretics. Antihypertensive effect diminished
by indomethacin, salicylates, NSAIDs.
Doxazosin mesylate.
Hypertension. Urinary outflow obstruction & symptoms
associated w/ benign prostatic hyperplasia.
pregnancy, lactation. Impaired liver function.
Dizziness, headache, fatigue, postural dizziness, vertigo,
oedema, asthenia.
Perindopril.
essential hypertension, CHF.
Pregnancy, lactation; childn.
Renal failure; renovascular hypertension; surgery/anesth;
elderly. Hemodialysis: avoid combination w/ highly permeable
membranes (polyacrylonitrile).
GI disorders; dizziness, headaches, mood &/or sleep
disorders, asthenia; taste disorder; cramps, localized skin
rashes; dry cough; angioneurotic edeme.
K supplements or K-sparing diuretics may induce hyperkalemia
esp in renal failure. Neuroleptics or imipramine-like antidepressants
increase risk of postural hypotension. Serum lithium conc
may rise during lithium therapy.
Losartan.
Hypertension.
Pregnancy.
Intravascular vol depletion. Cirrhosis & hepatic
impairment. Bilateral renal artery stenosis or stenosis
of the artery to a solitary kidney. Changes in renal function.
Lactation & childn.
Abdominal pain, asthenia/fatigue, chest pain, oedema/swelling,
palpitation, tachycardia, diarrhoea, dyspepsia, nausea,
back pain, muscle cramps, dizziness, headache, insomnia,
cough, nasal congestion, pharyngitis, sinus disorder, upper
resp infection, angioedema, hepatitis, liver function abnormalities,
myalgia, migraine, urticaria, pruritus.
Concomitant use of K-sparing diuretics, K supplements/salt
substitutes containing K may lead to increases in serum
K.
Delapril HCI.
Essential, renal or renovascular hypertension.
Patients w/ a history of angioneuratic edema to other
ACE inhibitors.
Patients w/ serious renal impairment or bilateral renal
arteriostenosis; peptic ulcer or gastric disease; epilepsy
or Huntington’s chorea. Patients should not be given
w/ in 24 hr before surgical operation, pregnancy, lactation,
childn. May impair ability to drive or operate machinery.
Occasionally, dizziness, lightheadedness, headache,
insomia, stiff shoulder; nausea, vomiting, anorexia, coughing,
hypersensitivity reactions; hot flushes, palpitations; hematological
effects; malaise, diaphoresis, weakness, pharyngalgia.
May cause increase in serum K in combination w/ K-sparing
diuretics. Enhancement of BP-lowering effects when used
w/ other antihypertensive drugs.
Valsartan.
Hypertension.
Pregnancy.
severely Na or vol-depleted patients. Bilateral or unilateral
renal artery stenosis. Hepatic insufficiency or biliary
obstructive disorders. Caution when driving or operating
machinery. Childn. Lactation.
Headache, dizziness, viral infection, upper resp tract
infection, coughing, diarrhea, fatigue, rhinitis, sinusitis,
back pain, abdominal pain, nausea, pharyngitis, arthralgia.
Concomitant use of K-sparing diuretics, K supplements
or salt substitutes containing K may lead to increases in
serum K.
Losartan K 50mg, hydrocholorothiazide 12.5mg.
treatment of hypertension, for patients in whom combination
therapy is appropriate.
Intravascularly volume-depleted, severe renal impairment,
hepatic impairment, anuria, hypersensitivity to other sulfonamide-derived
drugs. Pregnancy.
Lactation. Childn.
Dizziness, angioedema, diarrhoe.
Concomitant use of K sparing diuretics, K supplements/salt
substitutes containing K. Hydrochlorothiazide may interact
w/ the following: alcohol, barbiturates, narcotics, antidiabetic
agents, other antihypertensives, cholestyramine, colestipol
resins, corticosteroids, ACTH, pressor amines, skeletal
muscle relaxants, Lithium, NSAIDs.
Prazosin HCI.
Hypertension, benign prostatic hyperplasia
Left ventricular failure due to mechanical obstruction.
Hypersensitivity. Childn <12 yr.
pregnancy & lactation.
Postural hypotension, headache. GI upsets, incontinence,
edema, impotence, tinnitus, dry mouth, nasal congestion.
Additive hypotensive effect w/ diuretics or other antihypertensives.
Fosinopril Na.
Hypertension. Treatment of heart failure in combination
w/ a diuretic.
Hypersensitivity. History of angioneurotic edema related
to previous treatment w/ an ACE inhibitor. Pregnancy.
Impaired renal function. Hypotension, hyperkalaemia.
Surgey/anesth.
dizziness, cough, upper resp symptoms, GI disturbances,
palpitations/chest pain, rash/pruritus, musculoskeletal
pain/paresthesia, fatigue, taste disturbance.
exaggerated hypotension response when used w/ diuretics.
Absorption may be impaired by antacids. NSAIDs may interfere
w/ the antihypertension effect of the drug. May increase
serum lithium conc. Effects potentiated when used w/ other
antihypertensives.
Indapamide.
essential hypertension.
Hypersensitivity to sulfonamides; severe hepatic or
renal failure, hepatic, encephalopathy, hypokalemia.
Pregnancy & lactation. Serum monitoring of K &
uric acid in those predisposed to hypokalaemia or gout.
Patients w/ a history of allergy to sulfonamide derivatives
should be closely monitored.
fatigue, orthostatic hypotension, hypokalaemia, allergic
manifestations.
Lithium, nonarrhythmia (astemizole, bepridil, IV erythromycin,
halofantrine, pentamidine, sultopride, terfenadine, vincamine).
Enalapril maleate.
Hypertension. Heart failure & prevention of coronary
ischemic events in patient w/ left ventricular dysfunction.
Prevention of symptomatic heart failure.
History of angioneurotic edema related to previous treatment
w/ an ACE inhibitor.
Symptomatic hypotension may occur. Vol or salt-depleted
patients & those w/ ischemic heart or cerebrovascular
disease. Patients undergoing major surgery or during anesth
w/ agents that produce hypotension. In patients w/ renal
impairment or renal artery stenosis, lower doses &/or
reduce frequency may be required. History of angioedema
unrelated to ACE inhibitor may be at increased risk of angioedema.
Use in pregnancy may lead to oligohydramnious & deformations.
Lactation. Childn.
Dizziness, headache, diarrhea, fatigue, asthenia, cough,
orthostatic hypotension; hyperkalemia; angioneurotic edema
(discontinue therapy).
May have additive effects w/ other antihypertensives,
K supplement, K-sparing diuretics, or K-containing salt
substitutes. Lithium lenels may increase if used together
w/ Renitec.
Atenolol 50mg, chlorthalidone 12.5mg.
Hypertension.
Presence of 2nd or 3rd degree heart block, cardiogenic
shock. Bradycardia, hypotension, metabolic acidosis, severe
peripheral circulatory disturbances, sick sinus syndrome,
untreated phaeochromocytoma, uncontrolled heart failure.
Poor cardiac reserve, overt heart failure, COPD or asthma.
W/drawal of ß-blockers should be gradual in patients
w/ ischemic heart disease. Peripheral arterial circulatory
disorders. History of anaphylaxis to a variety of allergens.
Renal impairment, diabetes mellitus. Pregnancy & lactation.
Monitor K levels. 1st degree heart block, Prinzmetal’s
angina, thyrotoxicosis, hypoglycemia. May impair ability
to drive or operate machinery. Hypokalaemia, hyperuricaemia.
Cold extremities, fatigue, GI disturbances bradycardia.
Occasionally, deterioration of heart failure, headache,
mood changes, confusion, nightmare, dizziness. Rarely sleep
disturbances, alopecia, thrombocytopenia, purpura, psoriasiform
skin reactions, exacerbation of psoriasis, visual disturbances,
psychoses, hallucinations, heart block, postural hypotension
which may be associated w/ syncope. Rashes & dry eyes
(discontinue drug). Rashes, dry eyes have been reported
w/ ß-blockers; chlorthalidone may cause nausea, dizziness;
rarely idiosyncratic reaction eg thrombocytopenia &
leucopenia. Hyperuricaemia, hypokalaemia, impaired glucose
tolerance, intermittent claudication, Raynaud’s phenomenon.
Paraesthesia.
Ca-channel blockers eg verapamil or diltiazem, lithium,
digitalis or Class 1 antiarrhythmic agents. Diuretics may
cause hyperuricaemia. Sympathomimentic agents, prostaplandin
synthetase inhibitors, anesth agents. Concomitant use w/
dihydropyridine may increase risk of hypotension.
Ramipril.
Hypertension, Post MI
Hereditary angioneurotic edema. Pregnancy. Lactation.
Impaired renal or liver function.
Nausea, dizziness & headache, dry cough. Hypersensitivity
reactions including pruritus, rash & fever.
Additive effects w/ other antihypertensives, increased
serum K when used w/ K-sparing diuretics. Concomitant administration
w/ lithium salts may increase serum lithium concentration.
Lisinopril dihydrate.
Hypertension, CHF, Acute MI, renal complications of diabetes
mellitus.
Angioedema associated w/ ACE inhibitors & in patients
w/ hereditary or idiopathic angioedema.
Symptomatic hypotension particularly in vol-depleted
patients & CHF. Hypotension may occur during surgery/anesth.
Patients w/ ischemic heart or cerebrovascular disease. Aortic
stenosis or hypertrophic cardiomyopathy. Renal impairment.
History of angioedema. Pregnancy, lactation. Anaphylactoid
reactions reported in patients undergoing hemodialysis &
desensitization treatments.
Dizziness, headache, diarrhoea, fatigue, cough, nausea,
rash, orthostatic effects, asthenia. Rarely, angioedema,
MI, CVA possibly secondary to excessive hypotension in high
risk patients, palpitations, tachycardia, abdominal pain
and indigestion, dry mouth, hepatitis, jaundice, vomiting,
mood alterations, mental confusion, vertigo, urticaria,
diaphoresis, uraemia, oliguria/anuria, renal dysfunction,
acute renal failure, impotence, a symptom complex which
may include fever, vasculitis, myalgia, arthralgia/arthritis,
positive ANA, elevated ESR, eosinophilia & leukocytosis.
Rash, photo-sensitivity or other dermatological manifestations.
Increases (usually reversible) in blood urea, serum creatinine,
liver enzymes & serum bilirubin. Small decreases in
hemoglobin & hematocrit. Hyperkalemia, hyponatremia,
leucopenia, thrombocytoprnia, bone marrow depression, manifest
as anaemia, paraesthesia, pancreatitis. Rarely, haemolytic
anaemia.
Risk of hyperkalemia w/ K-sparing diuretics, K supplements,
K-containing salt substitutes. Antihypertensive effect may
be diminished bu indomethacin. Additive antihypertensive
effects w/ diuretics. May reduce lithium elimination. ACE
inhibitors may potentiate the hypoglycaemic effect of insulin
& oral anti-diabetic drugs.
d) Beta Blockers
metoprolol tartrate.
Hypertension, angina pectoris.
AV block II & III, uncompensated cardiac failure,
cardiogenic shock, marked bradycardia.
Treatment should be w/ drawn graduallt. For patients
undergoing elective surgery, employ a ß-blocker as
premed. Cardiac decompensation. Pregnancy & lactation.
lassitude, GI & sleep pattern disturbances; rarely,
non-specific skin reactions & coldness of extremities.
increased risk of myocardial depression w/ verapamil,
diltiazem & Class I antiarrhythmics
Bisoprolol fumarate.
Hypertension, CHD (angina pectoris).
Untreated myocardial failure, shock, AV block grades
II & III, sick sinus syndrome, SA block, dradycardia
w/ <50 beat/min; bronchial asthma, hypotension, advanced
stages of peripheral circulatory disturbance; pheochromocytoma
w/o concomitant, adrenoceptor blocking therapy. Pregnancy,
lactation; childn.
Diabetic patients w/ greatly fluctuating blood-sugar
values, during prolonged periods of fasting; acidosis. Prior
operation as cardiac output may be impaired under anaesth.
At start of treatment but generally recede w/in 1-2
wk treatment: rare: GI disturbances, skin reactions, decreased
BP, slow pulse rate, AV conduction disturbance, cold extremities,
muscle weakness/cramp & reduced lacrimation. May aggravate
intermittent claudication & Raynaud’s phenomenon,
intensify myocardial failure, increase airway resistance,
impair glucose tolerance, mask signs of low sugar levels.
Tiredness, dizziness, slight headache, perspiration, sleep
disturbancesm vivid dreams & depressive moods.
Reserpine, methyldopa, clonidine, guanfacine, nifedipine,
rifampicin, Ca-antagonist of the verapamil & diltiazem
type, antiarrhythmics, insulin or oral bllod sugar-reducing
drugs.
Propranolo HCI.
Hypertension, Angina, anxiety, migraine & essential
tremor, dysrhythmias, anxiety, tachycardia, hypertrophic
obstructive cardiomyopathy & thyrotoxicosis, LA Hypertension,
thyrotoxicosis. Prophylaxis of angina pectoris & migraine.
Prophylaxis after acute MI
2nd or 3rd degree heart block, cardiogenic shock, overt
heart failure, history of bronchospasm, prolonged fasting,
metabolic acidosis.
poor cardiac reserve be gradual in patients w/ ischemic
heart disease. W/drawal of clonidine. Pregnancy & lactation.
Caution in hepatic or renal impairment, decompensated cirrhosis,
peripheral arterial circulatory disorders & in patients
w/ history of anaphylaxis to a variety of allergens.
Cold extremities, GI & sleep disturbances; fatigue,
lassitude. Deterioration in heart failure, mood changes,
isolated cases of paraesthesia. Rarely, bradycardia, heart
block, alopecia, thrombocytopenia, purpura, psoriasiform
skin reactions, exacerbation of psoriasis. CNS symptoms
including hallucinations.
Ca-channel blockers eg verapamil or diltiazem. Class
I antiarrhythmic agents, ergotamine or dihydroergotamine,
indomethacin, chlorproamazine or parenteral adrenaline or
parenteral lignocaine.
Betaxolol HCI
Arterial hypertension.
Cardiogenic shock, uncontrolled congestive cardiac failure,
2nd or 3rd degree AV block if no pacemaker is present. Marked
bradycardia (heart rate <50 beats/minute).
1st degree AV block; asthma; Raynaud’s disease;
hypertension due to pheochromocytoma; diabetics prone to
hypoglycemia.
Lassitude, exacerbation of Raynaud’s disease or
intermittenet claudication & paraesthesia of extremities.
Marked bradycardia, hypertension, AV block, cardiac insufficiency
& bronchospasm.
Myocardial depressants or drugs depressing AV conduction.
Clonidine should not be continued until several days after
w/drawal of ß-blocker.
Atenolol.
Hypertension, angina pectoris & cardiac dysrthythmias,
MI
presence of 2nd or 3rd degree heart block; cardiogenic
shock. Bradycardia, hypotension, metabolic acidosis, severe
peripheral circulatory disturbances, sick sinus syndrome,
untreated phaeochromocytoma, uncontrolled heart failure.
poor cardiac reserve, overt heart failure, COPD or asthma,
avoid abrupt cessation of therapy in ischemic heart disease.
May aggravate peripheral arterial circulatory disorders.
History of anaphylactic reaction. Anaesth. W/drawal of clonidine.
Pregnancy & lactation. Modifies tachycardia of hypoglycemia.
Cold extremities, nuscccular fatigue, GI disturbances,
bradycardia, headache, mood changes, heart failure, sleep
disturbances, alopecia, skin rashes, dry eyes, thrombocytopenia,
purpura, psoriasiform skin reactions, exacerbation of psoriasis,
heart block.
Combines use w/ Ca-channel blockers w/ -ve inotropic
effects eg verapamil or diltiazem. Modifies the tachycardia
of hypoglycaemia. Sympathomimetic agents, prostaglandin
synthetase inhibitors, anesth agents. Concomitant use w/
dihydropyridine may increase risk of hypotension. Class
I antiarrhythmic agents eg. disopyramide, digitalis glycosides.
e) Calcium Antagonists
Nifedipine.
Stable angina pectoris, post-infarct angina, hypertension.
CV shock; pregnancy & lactation.
Severe hypotension; close monitoring of dialysis patients
w/ malignant hypertension; heart failure, severe aortic
stenosis.
Initially mild & transient vasodilatation, hypotensive,
rarely GI, skin & otherreactions. Very rarely: chest
pain (if relationship established, discontinue therapy).
Extremely rare: on prolonged use gingival hyperplasia, gynaecomastia
(both regressing on discontinuation); temporary hyperglycarmia,
liver function disturbances (including intrahepatic cholestasis).
Ability to drive or operate machinery may be impaired.
Effect enhanced by antihypertensive agents, cimetidine
& ß-receptor blockers. Digoxin, quinidine (monitor
plasma level).
Verapamil HCI.
Chronic hypertension, Isoptin SR, Tab chronic stable
& unstable angina, angina at rest including vasospastic
angina; angina pectoris after IM; prophylaxis of supraventricular
tachyarrhythmias, Amp Hypertensive crises, treatment of
supraventricular tachyarrhythmias, acute coronary insufficiency(coronary
spasms)
CV shock, complicated acute MI, severre conduction disorders
(2nd & 3rd degree AV block, sinoatrial block), sick-sinus
syndrome, heart failure, atrial fibrillation/ flutter &
simultaneous pre-excitation syndrome. Myasthenia gravis.
1st degree AV block, bradycardia, hypotension. May impair
ability to drive or operate machinery. Pregnancy, lactation.
Severe impairment of liver function. Slows down markedly
the elimination of alcohol & prolongs the duration of
alcohol.
Constipation, dizziness, nausea. Rarely, vertigo, headache,
hypotension, ankle edema, flushing, fatigue, nervousness,
erythromelalgia, paraesthesia, neuropathy; bradycardiac
arrhythmias, CHF, dyspnea, raised prolactin levels, single
cases of galactorrhea. Very rarely. Myalgia, arthralgia,
allergi skin reactions; purpura, photosensitization dermatitis,
gynecomastia, reversible increase in transaminases &/or
alkaline phosphatase, relevant impairment of glucose tolerance;
gingival hyperplasia. Tachycardia, palpitations, impotence.
Tinnitus, tremor. Caution should be taken in patients w/
a pacemaker or defibrillator (possible increase insensing,
pacing & fibrillation threshold).
Effects enhanced by ß-blockers, antiarrhythmics
or inhalation anesth. May intensify effects of other antihypertensives.
Lithium (attenuated by verapamil, enhanced neurotoxicity).
Increases plasma level of cyclosporine. Theophylline, digoxin,
carbamazepine. Effects attenuated by rifampicin, phenytoin
& Phenobarbital. Effects of muscle relaxants may be
potentiated. Rise in plasma levels by grapefruit juice &
cimetidine. May increase plasma conc of certain ß-blockers
(atenolol, metoprolol, propranolol), quindine, prazosin,
midazolam, aspirin (increased risk of bleeding), alcohol
(reduced metabolism, increase in plasma levels).
Amlodipine besylate.
Hypertension & angina.
Known sensitivity to dihydropyridines.
Pregnancy & lactation; impaired liver function.
Headache, edema, fatigue, somnolence, nausea, abdominal
pain, flushing, paipitations, dizziness.
Felodipine.
Hypertension, stable angina pectoris.
Pregnancy including the early stages, lactation, levercirrose.
Flushing, headache, palpitations, dizziness, fatigue,
peripheral oedema.
Cimetidine, erythromycin, itraconazole cause an increase
in plasma conc. Phenytoin, carbamazepine, barbiturates will
cause a decrease in plasma conc.
g) Peripheral Vasodilators & Cerebral Activators
Cinnarizine diHCI.
Dizziness, imbalance, ear buzzing due to vestibular disorder,
peripheral & cerebral circulatory disorders.
Pregnancy.
Rarely, somnolence & GI disturbances. Aggravation
or appearance of extrapyramidal symptoms (prolonged use
in elderly).
Ginkgo biloba extr (EGB 761).
cerebral circulatory insufficiency. ENT, circulatory,
neurosensory disorders (tinnitus, vertigo, dizziness). Peripheral
vascular disorders.
Rarely, digestive disturbances; rashes; headache.
h) Migraine Drugs
Ergotamine tartrate 1 mg, caffeine 100mg.
Acute migraine attack & related types of vascular
headache.
Impaired peripheral circulation, obliterative vascular
disease, CHD; severe hypertension; renal or hepatic insufficiency,
sepsis; pregnancy, lactation.
Avoid frequent & prolonged use, discontinue treatment
in impaired peripheral circulation. During prolonged &
uninterrupted treatment drug-induced headache & rare
case of rectal or anal ulcer occurred.
Nausea, vomiting; paresthesia, pain & weakness in
the extremities; peripheral vasoconstriction (discontinue
drug). Precordial pain, myocardial ischaemia & infarction.
Prolonged use may cause pleural or retroperitoneal fibrosis
or fibrotic changes in the cardiac valves.
possible risk of peripheral ischemia w/ erythromycin,
troleandomycin, josamycin. Enhanced risk of vasospastic
reaction w/ propranolol (rare). Vasoconstrictor agents.
Sumatriptan succinate.
Acute relief of migraine w/ or w/o aura (tab/inj) &
cluster headache (inj only).
Ischaemic heart disease, previous MI, Prinzmetal’s
angina. Uncontrolled hypertension. MAOI therapy. Peripheral
vascular disease or patients who have symptoms or signs
consisitent w/ IHD. History of CVA or transient ischaemic
attack. Severe hepatic impairment. Inj should not be given
IV.
May impair ability to drive or operate machinery. Conditions
predisposed to ischaemic heart disease. Hepatic or renal
impairment. Controlled hypertension.
Transient pain at inj site. Sensations of tingling,
heat, heaviness, pressure or tightness in any part of the
body, flushing, dizziness & feeling of weakness. Fatigue
& drowsiness. Nausea & vomiting. Transient increase
in Bp. Visual disorders.
Ergotamine, MAOIs, 5-HT receptor inhibitors, lithium.
i) Anticoagulants, Antithrombotics & Fibrinolytics
Recombinant human tissue-type plasminogen activator.
Thrombolytic treatment in acute MI (AMI): 90 mins (accelerated
dose regimen for patients in whom treatment can be started
w/ in 6 hr of symptom onset; 3 hr dose regimen for patients
in whom treatment can be started between 6-12 hr after symptom
onset. Thrombolytic treatment in acute massive pulmonary
embolism w/ haemodynamic instability.
Known haemorrhagic diathesis, patient receiving oral
anticoagulants, manifest or recent severe or dangerous bleeding,
history of stroke or CNS damage, haemorrhagic retinopathy,
recent (< 10 days) traumatic external heart massage,
obstetrical delivery, recent puncture of a non-compressible
blood vessel, severe uncontrolled arterial hypertension,
bacterial endocarditis, pericarditis acute pancreatitis,
documented ulcerative GI disease during the last 3 mth,
oesophageal varicosis, arterial aneurisms, arterial/ venous
malformations. Neoplasm w/ increased bleeding risk, severe
liver disease, including hepatic failure, cirrhosis, portal
hypertension (oesophageal varices) & active hepatitis,
major surgery or significant trauma in past 10 days
Smaller, recent traumas, such as biopsies, puncture
of major vessel, IM inj, cardiac massage for resuscitation.
Condition which increased bleeding tendencies & elderly
patient.
Superficial & internal bleeding.
Anticoahulants & antiplatelet agents increase danger
of bleeding.
Tirofiban HCI
used in combination w/ heparin for patients w/ unstable
angina or non-Q-wave MI to prevent cardiac ischemic events
& is also indicated for patients w/ coronary ischemic
syndromes undergoing coronary angioplasty or atherectomy
to prevent cardiac ischemic complications related to abrupt
closure of the treated coronary artery.
Hypersensitivity; active internal bleeding; history
of intracranial hemorrhage; intracranial neoplasm, arteriovenous
malformation or aneurysm; patients who developed thrombocytopenia
following prior exposure to Aggrastat.
Recent (<1yr) bleeding, including a history of GI
bleeding or genitourinary bleeding of clinical significance;
known coagulopathy, platelet disorder or history of thrombocytopenia;
platelet count < 150,000 cells/mm3; history of cerebrovascular
disease w/in 1 yr; major surgical procedure or severe physical
trauma w/in 1 mth history, symptoms or findings suggestive
of aortic dissection; severe uncontrolled hypertension (systolic
BP > 180 mmHg &/or diastolic BP> 110 mmHg); acute
pericarditis; hemorrhagic retinopathy; arterial access for
femoral sheath placement; severe renal insufficiency (creatinine
clearance <30 mL/Min). pregnancy, lactation, childn.
Risk of bleeding; nausea; fever; headache.
Drugs that affect hemostasis (eg warfarin).
Ticlopidine HCI.
Secondary prevention of cerebral & cardiovascular
occlusive ischaemia in patients w/ thrombotic risk. Prevention
of aorta-coronary bypass graft acclusion, in extracorporal
circulation, in haemodialysis & in thrombosis of central
vein of the retina.
Leucopenia, thrombocytopenia agranulocytosis, bleeding
diatheses, haemostatic disorders, Active pathological bleeding
(such as bleeding, GI ulcer, bleeding esophageal varices).
Acute haemorrhagic cerebrovascular strokes. Severe hepatopathy.
Pregnancy, lactation.
Every 15 days for the 1st 3 mths of treatment. To perform
blood cell counting. Treatment should be immediately w/drawn
when pharyngitis, ulcers of the buccal mucosa, angina, fever
bleeding or hematomas occur. History of drug abuse.
Leucopenia, thrombocytopenia, GI discomfort, increase
of transaminases & rarely cholestatic jaundice.
NSAIDs, anticoagulants.
Enoxaparin Na.
prophylaxis & treatment of thromboembolic disorders
of venous origin, particularly in moderate to high risk
orthopedic or general surgery. Prevention of thrombosis
in extracorporeal circulation during hemodialysis.
History of thrombocytopenia during enoxaparin therapy.
Hemorrhagic tendencies, organic lesion w/tendency to bleed,
major blood clotting disorder. Acute infectious endocarditis,
hemorrhagic stroke syndrome, acute GI ulcer.
Liver or kidney failure, uncontrolled arterial hypertension,
history of GI ulcer, vascular diseases of the choroids &
retina. Post-op period following surgery of brain &
spainal cord. History of thrombocytopenia occurring w/ another
heparin. 1st trimester of pregnancy. Do not give by IM route.
Hemorrhagic symptoms, thrombocytopenia (rare0, hematomes
& skin necrosis at inj site; skin allergies or systemic
allergic reactions.
Increased risk of hemorrhage when used w/ NSAIDs, ticlopidine,
corticosteroids, dextran 40. May potentiate effects of oral
anticoagulants. Vit K antagonists, anti-platelet drugs.
Warfarin Na.
Venous thrombosis 7 its extension, atrial fibrillation
w/ embolization, pulmonary embolism & as adjunct in
treatment of coronary occlusion.
Pregnancy; haemorrhagic tendency or blood dyscrasias;
recent or contemplated surgery of CNS, eye; traumatic surgery
resulting in large open surfaces; bleeding tendencies associated
w/ active ulceration or overt bleeding; threatened abortion;
spinal puncture.
Haemorrhage. Periodic determination or prothrombin time
is essential. Necrosis &/or gangrene of skin & other
tissue. Known or suspected hereditary, familial or clinical
deficiency in protein has been associated w/ an increased
risk of developing necrosis during warfarin administration.
Also see lit.
Harmorrhage, necrosis of skin or other tissues. Infrequently,
alopecia, urticaria, dermatitis, fever, GI disturbances,
abdominal cramps, ‘purple toes’ syndrome, cholestatic
hepatic injury. Hypersensitivity reactions.
Effects diminished by barbiturates, cholestyramine,
glutethimide, rifampicin, vit K, griseofulvin, carbamazepine,
ethchlorvynol. Effects enhanced by phenylbutazone, anabolic
steroids, chloral hydrate, cimetidine, clofibrate, d-thyroxine,
diflunisal, disulfiram, mefenamic acid, metronidazole, quinidine.
Interferes w/ metabolism or excretion of hypoglycemic agents
& anticonvulsants.
Nadroparin Ca low molecular wt.
prophylaxis & treatment of thromboembolic disorders.
previous thrombocytopenia w/ nadroparin therapy, signs
or increased risk of hemorrhage associated w/ hemostasis
disorders except for disseminated intravascular coagulation
not induced by heparin, organic lesion likely to bleed,
hemorrhagic CVA, acute infective endocarditis.
hepatic or renal insufficiency, uncontrolled arterial
hypertension, history of peptic ulceration, vascular chorioretinal
disorder; post-opbrain, spinal cord or eye surgery.
Overt or concealed hemorrhage; rarely, severe thrombocytopenia,
small hematoma, cutaneous necrosis at inj site; raised transaminases,
hypoaldosteronism.
NSAIDs, aspirin, oral anticoagulants, antiplatelet agents,
dextrans.
Heparin Na.
prophylaxis & treatment of venous thrombosis &
pulmonary embolism. Treatment of MI & arterial embolism.
For prevention of clotting in arterial & heart surgery
& prevention of cerebral thrombosis. As an anticoagulant
in blood transfusions, extracorporal circulation, dialysis
& for lab purposes.
Hemorrhagic diseases, thrombocytopenia, hemoplilia;
subacute bacterial endocarditis; peptic ulcer; severe hypertension;
patient who has recently undergone surgery at site where
hemorrhage is a special risk.
Elderly, pregnancy. Increased resistance is frequently
encountered in thrombosis, thrombophlebitis infected w/
thrombotic tendencies, cancer, post-surgical patients, advanced
renal or hepatic disease, jaundice.
Transient alopecia, diarrhea; osteoporosis w/ spontaneous
fractures. Occasionally, febrile or allergic reactions.
Drugs that interfere w/ platelet-aggregation reaction
may induce bleeding. Digitalis, tetracyclines, nicotine
or antihistamines may partially counteract the anticoagulant
actions
Purified streptokinase.
Acute MI, deep venous thrombosis, pulmonary embolism,
arterial occlusions, intrapleural adhesions, thrombosis
of tricuspid valve prosthesis & in haemodialysis shunts.
Recent trauma or traumatic procedures; cerebral arterial
disease; potential or active bleeding; potential cardiac
emboli; recent strepto-kinase therapy; severe uncontrolled
hypertension; hypertensive or diabetic nephropathy, recent
CV events w/in last 2 mth; haemorrhagic diathesis.
Advanced age; IM inj.
Febrile & allergic reactions; hemorrhage; hypotension,
bradycardia.
Anticoagulant & antiplatelet agents increase risk
of bleeding.
Clopidogrel.
Reduction of artherosclerotic events (MI, stroke &
vascular death) in patients w/ artherosclerosis documented
by recent stroke, recent MI or established peripheral arterial
disease.
Severe liver impairment. Peptic ulcer & intracranial
haemorrhage. Lactation.
Patients who may be a risk of increased bleeding from
trauma, surgery or other pathological conditions. Patients
w/ moderate hepatic disease who may have bleeding diatheses.
Pregnancy.
GI bleeding, purpura, bruising, haematoma, epistaxis,
haematuria, eye bleeding, intracranial bleeding, abdominal
pain, dyspepsia, gastritis * constipation, rash, pruritus.
Warfarin, aspirinm heparin, thrombolytics or NSAIDs.
Abciximab.
Adjunct to heparin & aspirin for: the prevention
of ischemic cardiac complications in patients undergoing
percutaneous coronary intervention (balloon angioplasty,
atherectomy & bail out stent); the short-term (1 mth)
reduction o9f the risk of MI, in patients w/ unstable angina,
not responding to full conventional therapy who have been
scheduled for percutaneous coronary intervention.
Active internal bleeding; history of CVA w/in 2 yr;
recent intracranial or intraspinal surgery or trauma; recent
major surgery; interacranial neoplasm, arteriovenous malformation
or aneurysm; know bleeding diathesis or severe uncontrolled
hypertension; pre-existing thrombocytopenia; vasculitis;
hypertensive or diabetic retinopathy; severe hepatic or
renal failure.
In case of bleeding or thrombocytopenia, discontinue
therapy. Puncture of major vessels, IM inj. Pregnancy, lactation.
Bleeding, thrombocytopenia; human anti-chimeric antibody
(HACA) development; hypotension; nausea & vomiting;
back pain; chest pain; headache; bradycardia; fever, puncture
site pain.
Increased risk of bleeding w/ heparin, other anticoagulants,
thrombolytics & antiplatelet agents.
j) Haemorrhoidal, Phlebitis & Varicose Preparations
Micronised purified flavonoidic fraction (diosmin 450mg,
heperidin 50 mg).
Organic & functional chronic venous insufficiency
of the lower limbs; heavy legs, pain, nocturnal cramps.
Hemorrhoidal disease, acute hemorrhoidal attracks.
Lactation
Minor GI & neurovegetative disorders.
Standardized ginkgo bilooba extr containing 24% of Ginkgo
glycosides & 6% of Ginkgolides-bilobalide 0.014g, heptaminol
HCI 0.3g, troxerutin 0.3g.
Symptoms related to venolymphatic insufficiency eg varicose
veins, oedema, cramps, heavy legs, pain, restless legs.
Functional signs related to acute haemorrhoidal attack.
Hyperthyroidism; associated use w/ MAOIs (risk of hypertension).
Avoid simultaneous administration w/ MAOIs.
Per g oint Lupinus albus 71mg, vateria indica 71mg,
menthe piperita 56.7mg, Aloe vera 142mg. Per supp Lupinus
albus 107 mg, vateria indica 107mg, menthe piperita 85mg.
Aloe vera 214mg.
Relief of pain & itch of haemorrhoids.
Pregnancy.
Rarely, minor transient anal itching.
Per supp Tribenoside 400mg, lidocaine 40mg. cream tribenoside
5%, lidocaine HCI 2%.
External & internal haemorrhoids.
Pregnancy & lactation.
Slight burning sensation, pain, increased intestinal
motility.
Oint Hydrocortisone 0.5%, cinchocaine HCI 0.5%, framycetin
sulfate 1%, aesculin 1%. Supp Hydrocortisone 5mg, cinchocaine
HCI 5mg, framycetin sulfate 10mg, aesculin 10mg.
Haemorrhoids, anal fissure, inflammatory, pruritus.
Extensive use in infants or pregnancy.
Pentoxifylline.
Peripheral occlusive arterial disease, cerebrovascular
disorders, circulatory disorders of the inner ear.
pregnancy. Massive bleeding, extensive retinal bleeding.
Hypersensitivity to methylxanthines.
Severe cardiac arrhythmias, MI, hypotension, severely
impaired renal/liver function, increased bleeding tendency.
Lactation. Childn.
Flushes, GI discomfort, cardiac arrhythmias at high
dose. Pruritus, reddening of the skin, urticaria. Dizziness,
headache, agitation, sleep disturbances. Rarely, angina
pectoris, hypotension, increased bleeding tendency.
Antihypertensive agents, nitrates, insulin, oral antidiabetics,
theophylline, ketorolac.
k) Haematopoietic Agents
Recombinant human erythropoietin (r-Hu-Epo) or epoetin
alfa.
Treatment of symplomatic or transfusion required anaemia
associated w/ chronic renal failure (CRF). Treatment of
anaemia in cancer.
Uncontrolled hypertension, ischemic vascular disease,
history of seizures. Changes in Hb, BP & serum electrolytes.
Hb levels should be measured wkly until a stable level of
10-12g/dL is achieved & periodically monitored thereafter.
Hyperkalemia. Increased protein intake & clotting.
Increased BP, thrombosis of vascular access sites. Flu-like
symptoms, bone pain & chills after inj. Seizures. Skin
reactions, palpebral edema.
Potentiated by hematinic agents.
l) Other Cardiovascular Drugs
Ubidecarenone coenzyme Q10.
Stmptoms associated w/ mild & moderate CHF in patient
w/ standard treatment.
Infrequently, gastric discomfort, anorexia, diarrhea,
nausea, skin rash.
