CALAPTIN
ABBOTT
ABBOTT HEALTHCARE PVT LTD 271 BUSINESS PARK 6TH FLOOR MODEL INDUSTRIAL COLONY GOREGAON EAST MUMBAI 400063
Verapramil 40mg/80mg tablets,
Strength | Rate | Packing Style |
---|---|---|
40mg | 7.62 | 10s tablets |
80mg | 14.01 | 10s tablets |
List of Related Indications:
- Arrhythmias
- Supraventricular tachycardia
List Of Drugs:
- Verapramil( *** ) @ - Calcium Channel Blocker
Indication Type Description:
Drug Interaction
Indication
Adverse Reaction
Contra-Indications
Dosages/ Overdosage Etc
Patient Information
Pharmacology/ Pharmacokinetics
Interaction with Food
Pregnancy and lactation
Drug Interaction:
Calcium Channel Blockers include -
Bepridil, Diltiazem, Felodipine, Isradipine, Nicardipine, Nifedipine,
Nimodipine, Verapramil, Amlodipine, Nisodipine, Clevidipine, Lercandipine
Refer verapramil-
Interacting drugs - summary
+ Cal. Channl Blockers -
Barbiturates + Verapramil
Verapramil bioavailabilty decreased
Calcium salts + verapramil
clinical effects & toxicities of Verapramil reversed
Dantrolene + Verapramil
hyperkalaemia and myocardial depression occur.
Erythromycin + felodipine
pharmacologic and toxic effects of felodipine increased
H2 antogonists + Diltiazem/Felodipine/ Nicradipine/Nifedipine / verapramil /
cimetidine and ranitidine increase the bioavailability
of diltiazem, felodipine, and nicradipine.
Cimetidine increase Verapramil's bioavailability
Hydantoin + Felodipine/ Verapramil
serum felodipine and Verapramil levels increased
Quinidine + Verapramil/Nifedipine
Hypotension, bradycardia, ventricular arrhythmia,
AV block and pulmonary edema occur.
Use concomittantly only when no other alternatives exist.
Rifampicin + verapramil
loss of clinical effect of oral Verapramil occur,
IV verapramil circumvent the interaction
Sulfinpyrazone + Verapramil
increased clearance and decreased bioavailabilty
of verapramil occur
Vitamin D + Verapramil
therapeutic efficacy of verapramil reduced
Nifedipine + Anticoagulants
rarely increased prothrombin time.
Verapramil, Diltiazem + Carbamazepine
increased carbamazepine serum levels with toxicity occur. Nifedipine does not appear to interact.
Diltiazem/Nicardipine/verapramil + cyclosporine
increased cyclosporine levels with possible toxiciy occur
Verapramil may be nephroprotective when given before cyclosporine. Monitor Cyclosporine levels
Bepridil/ Diltiazem/Felodipine/ Nifedipine /Verapramil + Digitalis Glycosides -
serum digitoxin levels increased.
Diltiazem + Encainide
serum encainide levels increased
Verapramil + Etomide
anesthetic effect of etomide increased with prolonged respiratory depression and apnea
Cal chan Blckrs + Fentanyl
severe hypotension or increased fluid volume occurred in patients receiving nifedipine.
Verapramil/ Diltiazem + lithium
reduction in lithium levels causing decreased antimaniac control,
Nifedipine + Mag sulphate Parentral
neuromuscular blockade and hypotension occurred with coadmin.
Verapramil + Non polarizing muscle relaxants
muscle relaxant effects may be enhanced. Respiratory depression prolonged
Verapramil + Prazosin
prazosin serum concentrations increased with increased sensitivity to prazosin.
Diltiazem/ Felodipine/ Nifedipine/Verapramil + Theophylline
pharmacologic actions of theophylline enhanced, with drug intoxication.
Theophylline levels slightly decreased.
Indication:
Angina
Calcium Channel Blockers include -
Bepridil, Diltiazem, Felodipine, Isradipine, Nicardipine, Nifedipine, Nimodipine, Verapramil, Amlodipine, Nisodipine, Clevidipine, Leracandipine
Refer Verapramil
Adverse Reaction:
Adverse reactions summary
Generally not serious, rarely requires discontinuation or dosage adjustment
VERAPRAMIL
CNS
Dizziness/lightheadeness 4%, Headache 2.%,
Asthenia , Insomnia 2 %
Weakness/shakiness ,Jitteriness, Parathesia, Somnolence, Confusion 1 %
GASTROINTESTINAL -
Constipation 7%, Nausea 3% ,
Diarrhea , Abdominal discomfort, Dry mouth/ thirst 1 %
CARDIOVASCULAR -
Hypotension 3%, Periph.edema 2%, Bradycardia 2 %,
Congestive heart failure, Pulmonary edema 2%,
AV block 1,2,3 degree 1%,
Palpitation, Syncope, Myocardial infarction < 1 %
DERMATOLOGIC -
Dermatitis/rash 1%, Erythema multiforme, Stevens-Johnson synd < 1%
HEMATOLOGIC -
Petechiae/ pupura/ bruising/ hematoma 1%
OTHER-
Shortness of breath/ dyspepsia/wheezing 2%,
Sweating 1%, Sexual difficultes,
Mituration disord, polyuria/nocturia/ frequency, Muscle cramps/ pain/inflammation 1 %
Lab test abnormalities-
Positive direct coombs test with or without hemolytic anemia with nifedipine.
Isolated cases of decreased platelet counts and elevated non-fasting serum glucose ,
LDH, alkaline phosphatase and ALT have occured with nimodipine. ALT increase with bepridil.
Some elevated liver function tests have occured with isradipine
Contra-Indications:
Cardiogenic shock,2nd or 3rd degree,
AV Block.Severe Badycardia,sick sinus syndrome.
Uncompensated heart failure. Acute phase of MI.
Special precautions:
1st degree AV block.Control poor cardiac reserve with digitalis and diuretics.
Bradycardia, conduction disturbances,atrial flutter/fibrillation with an accessory pathway. Hepatic impairment.
Pregnancy
Defective platelet function/thrombocytopenia.
Acute hepatic injury- in rare cases symptoms consistent with acute hepatic injury as well as significant elevations in enzymes such as alkaline phosphatae , CPK,LDH, AST, and ALT, have occured with diltiazem, and nifedipine.
Cholestatis with or without jaundice has occured with nifedipine. Rare instances of allergic hepatitis also occured with nifedipine
Warnings- Hypotension- carefully monitor blood pressure during initial administration and titration, closely monitor patients already taking hypertensives.
Congestive heart failure- CHF- has developed rarely, in patients receiving a beta-blocker after beginning nifedipine.
Use diltiazem, nicardipine, isradipine, felodipine, amlodipine and bepridil with caution in CHF patients
Antiplatelet effects- nifedipine decreases platelet aggregation in vitro.
Withdrawal syndrome- abrupt withdrawal of calcium channel blockers may cause increased frequency and duration of chest pain.Caution is warranted when discontinuing these drugs.
B-blocker withdrwal/nifediine- patients recently withdrawn from beta blockers may develop a withdrawal syndrome with increased angina,
Nicardipine- gradually reduce beta blocker dose over 8 to 10 days with coadministration.
Hepatic function impairment- the pharmocokinetics, bioavailability and patient response to verapramil and nifedipine may be significantly affected by hepatic cirrhosis
Renal function impairment- caution is adviced in use of these agents in such patients.
Elderly- verapramil, nifedipine and felodipine may cause a greater hypotensive effect than seen in younger patients, probably due to age-related changes in drug disposition.
Pregnancy- use during pregnancy only when clearly needed and when potential benefits outweigh potential hazards to the fetus.
Lactation- decidewhether to discontinue nursing or discontinue the drug while these agents are being used.
Children- Safety and efficacy of diltiazem, bepridil, felodipine, amlodipine and nifadipine have not been established.
Dosages/ Overdosage Etc:
Indications:
Angina,.arrhythmias,essential htpertension.
Dosage:
Angina- oral - initial dose 80 to 120 mg 3 times a day.
Overdosage- Symptoms
Nausea, weakness, dizzines, drowsiness, confusion and slurred speech. Marked and prolonged hypotension and bradycardia both of which may result in decreased cardiac output.
Death has occured.
Treatment
1. If the patient is shortly after oral ingestion employ emetics or lavage and carthartics
2. Beta-adrenergic agonists and IV calcium have been used effectively.
3. Treat cardiac failure with inotropic agents (isoproterenol, dopamine or dobutamine) and may not always reverse electrophysiologic toxicity.
4. Monitor cardiac and respiratory function, elevate the extremities.
5. Since these agents are highly protein bound dialysis is not likely to help. 6. Verapramil vannot be removed by dialysis
Missed dose-
1. If you miss a dose of this medicine, take it as soon as possible.
2. However, if it is almost time for next dose, skip the missed dose and go back to your regular dosing schedule.
3. Do not double doses.
Patient Information:
SPECIFIC INFORMATION-
Notify physician if any of following occur- Irregular heart beat, shortness of breath, swelling of the hands and feet, pronounced dizziness, constipation, nausea, or hypotension.
GENERAL
1.Take the medicine exactly as directed by the physician.
2.Swallow the tablet whole,without crushing or chewing it. However if advised by the doctor, you may break into half.
3.Take the medicine with food or milk.
4. Allergies- tell your if you ever had any allergic reactions to beperidil, diltiazem, felodipine,flunarizine, isradipine, nicardipine, nifedipine ,nimodipine or verapramil Tell your doctor if you are allergic to to any other substances such as foods, preservatives or dyes.
5. Pregnancy- calcium channel blockers have not been studied on pregnat women. Studies in animals have shown that large doses f calcium channel blockers cause birth defects , prolonged pregnacy poor bone development and stillbirth.
6. Breast feeding- pass into breast milk and cause problems to nursing babies
7. Children- no specific inforamtion available. Not expected to cause different side effects in children
8. Other medicines- Your Doctor should know what othher medicines to if you are taking so that he can advice you accordingly.
9. Other medical problems- Your doctor should be aware of your other medical problems. Heart rhythm problems - bepridil can cause serious heart rhythm problems Kidney disease or Liver disease -efects of calcium channel blockers may be increased .
10. Missed dose- If you miss a dose of this medicine take it as soon as possible. However, if it is almost time for the next dose skip the missed dose and go back to your regular dosing schedule. Do not double doses.
Pharmacology/ Pharmacokinetics:
Calcium Channel Blockers include -
Bepridil, Diltiazem, Felodipine, Isradipine, Nicardipine, Nifedipine,
Nimodipine, Verapramil, Amlodipine, Nisodipine, Clevidipine, Lercandipine
Interaction with Food:
Food may slow the rate but not the extent of nifedipine absorption
Administration of bepridil after a meal results in insignificant delay in time to peak concentration
Admin of isradipine with food significantly increases the time to peak by about an hour, but no effect on bioavailability
Admin of sustained release verapramil, with food increases time to peak, but bioavailability not affected Bioavailability of felodipine is affected by food
Bioavailabilty of amlodipine is not affected by food.
Pregnancy and lactation:
Pregnancy:
Use only when clearly needed.
Lactation:
Observe caution and decide whether to discontinue nursing or discontinue the drug.
Children:
Safety and efficacy have not been established.