Calcium channel blockers theophylline

Discontinue, if possible, drugs that may promote reflux (calcium channel blockers, /3-blockers, nitrates, theophylline). 

Drugs that may affect amiodarone include hydantoins, cholestyramine, fluoroquinolones, rifamycins, ritonavir, and cimetidine. Drugs that may be affected by amiodarone include anticoagulants, beta-blockers, calcium channel blockers, cyclosporine, dextromethorphan, digoxin, disopyramide, fentanyl, flecainide, hydantoins, lidocaine, methotrexate, procainamide, quinidine, and theophylline. Drug/Lab test interactions Amiodarone alters the results of thyroid function tests, causing an increase in serum T4 and serum reverse T3 levels and a decline in... 

Agents that may increase theophylline levels include allopurinol, beta blockers (nonselective), calcium channel blockers, cimetidine, oral contraceptives, corticosteroids, disulfiram, ephedrine, influenza virus vaccine, interferon, macrolides, mexiletine, quinolones, thiabendazole, thyroid hormones, carbamazepine, isoniazid, and loop diuretics. 

Drugs that might be affected by lopinavir/ritonavir include ergot derivatives, oral contraceptives, antiarrhythmics, HMG-CoA reductase inhibitors, HIV protease inhibitors, atovaquone, calcium channel blockers, ketoconazole, itraconazole, pimozide, cisapride, clarithromycin, disulfiram, metronidazole, immunosuppressants, midazolam, triazolam, narcotic analgesics, rifabutin and rifabutin metabolite, sildenafil, warfarin, bupropion, clozapine, desipramine, piroxicam, quinidine, theophylline, and zolpidem. 

In contrast, decreases in theophylline metabolism by selective inhibitors of CYP1A2, such as fluvoxamine and some quinolone antibiotics, or by selective and potent inhibitors of CYP3A4, such as the macrolide antibiotics, have resulted in serious theophylline toxicity (22). It is postulated that taken over time, the macrolide antibiotics act as mechanism-based inhibitors of CYP isoforms other than just CYP3A4. Some nonselective inhibitors of P450s, such as cimetidine, some p-blockers and calcium channel blockers, and others (19,22), also appear to inhibit the metabolism of theophylline enough to cause toxicity. 

DILTIAZEM, VERAPAMIL THEOPHYLLINE t theophylline levels with diltiazem and verapamil. Mostly not clinically significant but two cases of theophylline toxicity with verapamil have been reported Uncertain, but thought to be due to inhibition of CYP1A2-mediated metabolism of theophylline Be aware of the small possibility of theophylline toxicity when commencing calcium channel blockers check levels if any problems occur, and consider either reducing the dose of theophylline or using an alternative calcium channel blocker... 

B. Toxicodynamics Toxicodynamics is a term used to denote the injurious effects of toxins, ie, their pharmacodynamics. A knowledge of toxicodynamics can be useful in the diagnosis and management of poisoning. For example, hypertension and tachycardia are typically seen in overdoses with amphetamines, cocaine, and antimuscarinic drugs. Hypotension with bradycardia occurs with overdoses of calcium channel blockers, beta-blockers, and sedative-hypnotics. Hypotension with tachycardia occurs with tricyclic antidepressants, phenothiazines, and theophylline. Hyperthermia is most frequently a result of overdose of drugs with antimuscarinic actions, the salicylates, or sympathomimetics. Hypothermia is more likely to occur with toxic doses of ethanol and other CNS depressants. Increased respiratory rate is often a feature of... 

II. BRONCHODIIATORS - montelukast, theophylline 12. CARDIAC GLYCOSIDES -digitoxin 13. CALCIUM CHANNEL BLOCKERS - felodipine, nifedipine, nimodipine, nisoldipine, verapamil... 

Induction of hepatic metabolism 2. Inhibition of phenytoin metabolism (parecoxib - CYP2C9 calcium channel blockers -CYP3A4 mianserin -unknown) 3. Uncertain amiodarone inhibits CYP2C9, which plays a role in phenytoin metabolism and inhibits Intestinal P-gp, which may t bioavailability of phenytoin. Theophylline i absorption of phenytoin... 

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