Source:http://www4.wiwiss.fu-berlin.de/dailymed/resource/drugs/3767
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Diltiazem Hydrochloride (Capsule, Extended Release)
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| dailymed-instance:dosage |
Hypertensive or anginal patients who are treated with other formulations of diltiazem can safely be switched to diltiazem hydrochloride extended-release capsules (once-a-day dosage) at the nearest equivalent total daily dose. Subsequent titration to higher or lower doses may, however, be necessary and should be initiated as clinically indicated. Studies have shown a slight increase in the rate of absorption of diltiazem hydrochloride extended-release capsules (once-a-day dosage), when ingested with a high-fat breakfast; therefore, administration in the morning on an empty stomach is recommended. Patients should be cautioned that the diltiazem hydrochloride extended-release capsules should not be opened, chewed or crushed and should be swallowed whole.<br/>Dosage:<br/>Hypertension: Dosages must be adjusted to each patient's needs, starting with 180 mg or 240 mg once-daily. Based on the antihypertensive effect, the dose may be adjusted as needed. Individual patients, particularly���60 years of age, may respond to a lower dose of 120 mg. The usual dosage range studied in clinical trials was 180 mg to 480 mg once daily. Current clinical experience with the 540 mg dose is limited, the dose may be increased to 540 mg with little or no increased risk of adverse reactions. Doses should not exceed 540 mg once-daily. While a dose of diltiazem hydrochloride extended-release capsules given once-daily may produce an antihypertensive effect similar to the same total daily dose given in divided doses, individual dose adjustment may be needed.<br/>Angina: Dosages for the treatment of angina should be adjusted to each patient's needs, starting with a dose of 120 mg once-daily, which may be titrated to doses of up to 480 mg once-daily. When necessary, titration may be carried out over a 7 to 14 day period.<br/>Concomitant Use With Other Cardiovascular Agents:<br/>Sublingual Nitroglycerin: Sublingual Nitroglycerin may be taken as required to abort acute anginal attacks during diltiazem therapy.<br/>Prophylactic Nitrate Therapy: Diltiazem hydrochloride extended-release capsules (once-a-day dosage) may be safely coadministered with short- and long-acting nitrates.<br/>Beta-Blockers:<br/>Antihypertensives: Diltiazem has an additive antihypertensive effect when used with other antihypertensive agents. Therefore, the dosage of diltiazem hydrochloride or the concomitant antihypertensives may need to be adjusted when adding one to the other.
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Diltiazem is a calcium ion influx inhibitor (slow channel blocker or calcium antagonist). Chemically, diltiazem hydrochloride is 1,5-Benzothiazepin-4(5H)one,3-(acetyloxy)-5-[2-(dimethylamino) ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-, monohydrochloride, (+)-cis-. Its molecular formula is CHNOS HCl and its molecular weight is 450.99. Its structural formula is as follows: Diltiazem hydrochloride, USP is a white to off-white crystalline powder with a bitter taste. It is soluble in water, methanol and chloroform. Diltiazem Hydrochloride Extended-release Capsules, USP (Once-a-Day Dosage), for oral administration, contain multiple units of diltiazem hydrochloride extended-release 60 mg, resulting in the 120 mg, 180 mg or 240 mg dosage strengths allowing for the controlled release of diltiazem hydrochloride over a 24-hour period. In addition, each capsule contains the following inactive ingredients: ammonium hydroxide, colloidal silicon dioxide, dibutyl sebacate, D&C Yellow #10 aluminum lake, ethylcellulose, FD&C Red #40 aluminum lake, FD&C Blue #1 aluminum lake, FD&C Blue #2 aluminum lake, gelatin, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, n-butyl alcohol, oleic acid, pharmaceutical glaze, polyethylene glycol, propylene glycol, SDA-3A alcohol, sodium lauryl sulfate, synthetic black iron oxide and titanium dioxide. In addition, the 120 mg and the 180mg strengths contain D&C Red #28 aluminum lake. Diltiazem Hydrochloride Extended-release Capsules, USP (Once-a-Day Dosage) 120 mg, 180 mg and 240 mg meet USP Drug Release Test 8.
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The therapeutic benefits of diltiazem are believed to be related to its ability to inhibit the influx of calcium ions during membrane depolarization of cardiac and vascular smooth muscle.<br/>Mechanisms of Action:<br/>Hypertension: Diltiazem produces its antihypertensive effect primarily by relaxation of vascular smooth muscle with a resultant decrease in peripheral vascular resistance. The magnitude of blood pressure reduction is related to the degree of hypertension; thus hypertensive individuals experience an antihypertensive effect, whereas there is only a modest fall in blood pressure in normotensives.<br/>Angina: Diltiazem has been shown to produce increases in exercise tolerance, probably due to its ability to reduce myocardial oxygen demand. This is accomplished via reductions in heart rate and systemic blood pressure at submaximal and maximal work loads. Diltiazem has been shown to be a potent dilator of coronary arteries, both epicardial and subendocardial. Spontaneous and ergonovine-induced coronary artery spasm are inhibited by diltiazem. In animal models, diltiazem interferes with the slow inward (depolarizing) current in excitable tissue. It causes excitation-contraction uncoupling in various myocardial tissues without changes in the configuration of the action potential. Diltiazem produces relaxation of coronary vascular smooth muscle and dilation of both large and small coronary arteries at drug levels which cause little or no negative inotropic effect. The resultant increases in coronary blood flow (epicardial and subendocardial) occur in ischemic and nonischemic models and are accompanied by dose-dependent decreases in systemic blood pressure and decreases in peripheral resistance.<br/>Hemodynamic and Electrophysiologic Effects: Like other calcium antagonists, diltiazem decreases sinoatrial and atrioventricular conduction in isolated tissues and has a negative inotropic effect in isolated preparations. In the intact animal, prolongation of the AH interval can be seen at higher doses. In man, diltiazem prevents spontaneous and ergonovine-provoked coronary artery spasm. It causes a decrease in peripheral vascular resistance and a modest fall in blood pressure in normotensive individuals. In exercise tolerance studies in patients with ischemic heart disease, diltiazem reduces the double product (HR��SBP) for any given work load. Studies to date, primarily in patients with good ventricular function, have not revealed evidence of a negative inotropic effect. Cardiac output, ejection fraction and left ventricular end diastolic pressure have not been affected. Such data have no predictive value with respect to effects in patients with poor ventricular function. Increased heart failure has, however, been reported in occasional patients with pre-existing impairment of ventricular function. There are as yet few data on the interaction of diltiazem and beta-blockers in patients with poor ventricular function. Resting heart rate is usually slightly reduced by diltiazem. Diltiazem hydrochloride extended-release capsules produce antihypertensive effects both in the supine and standing positions. Postural hypotension is infrequently noted upon suddenly assuming an upright position. Diltiazem decreases vascular resistance, increases cardiac output (by increasing stroke volume), and produces a slight decrease or no change in heart rate. No reflex tachycardia is associated with the chronic antihypertensive effects. During dynamic exercise, increases in diastolic pressure are inhibited while maximum achievable systolic pressure is usually reduced. Heart rate at maximum exercise does not change or is slightly reduced. Diltiazem antagonizes the renal and peripheral effects of angiotensin II. No increased activity of the renin-angiotensin-aldosterone axis has been observed. Chronic therapy with diltiazem produces no change or an increase in plasma catecholamines. Hypertensive animal models respond to diltiazem with reductions in blood pressure and increased urinary output and natriuresis without a change in the urinary sodium/potassium ratio. In man, transient natriuresis and kaliuresis have been reported, but only in high intravenous doses of 0.5 mg/kg of body weight. Diltiazem-associated prolongation of the AH interval is not more pronounced in patients with first-degree heart block. In patients with sick sinus syndrome, diltiazem significantly prolongs sinus cycle length (up to 50% in some cases). Intravenous diltiazem hydrochloride in doses of 20 mg prolongs AH conduction time and AV node functional and effective refractory periods approximately 20%. In two short-term, double-blind, placebo-controlled studies, 303 hypertensive patients were treated with once-daily diltiazem hydrochloride extended-release capsules in doses of up to 540 mg. There were no instances of greater than first-degree atrioventricular block, and the maximum increase in the PR interval was .08 seconds. Nopatients were prematurely discontinued from the medication due to symptoms related to prolongation of the PR interval.<br/>Pharmacodynamics: In one short-term, double-blind, placebo-controlled study, diltiazem hydrochloride extended-release capsules (once-a-day dosage) 120, 240, 360 and 480 mg/day demonstrated a dose-related antihypertensive response among patients with mild to moderate hypertension. Statistically significant decreases in trough mean supine diastolic blood pressure were seen through four weeks of treatment: 120 mg/day (-5.1 mmHg); 240 mg/day (-6.9 mmHg); 360 mg/day (-6.9 mmHg); and 480 mg/day (-10.6 mmHg). Statistically significant decreases in trough mean supine systolic blood pressure were also seen through four weeks of treatment: 120 mg/day (-2.6 mmHg); 240 mg/day (-6.5 mmHg); 360 mg/day (-4.8 mmHg); and 480 mg/day (-10.6 mmHg). The proportion of evaluable patients exhibiting a therapeutic response (supine diastolic blood pressure<90 mmHg or decrease>10 mmHg) was greater as the dose increased: 31%, 42%, 48% and 69% with the 120, 240, 360 and 480 mg/day diltiazem groups, respectively. Similar findings were observed for standing systolic and diastolic blood pressures. The trough (24 hours after a dose) antihypertensive effect of diltiazem hydrochloride extended-release capsules (once-a-day dosage) retained more than one-half of the response seen at peak (3���6 hours after administration). Significant reductions of mean supine blood pressure (at trough) in patients with mild to moderate hypertension were also seen in a short- term, double-blind, dose-escalation, placebo-controlled study after 2 weeks of once-daily diltiazem hydrochloride extended-release capsules 180 mg/day (diastolic: -6.1 mmHg; systolic: -4.7 mmHg) and again, 2 weeks after escalation to 360 mg/day (diastolic: -9.3 mmHg; systolic: -7.2 mmHg). However, a further increase in dose to 540 mg/day for 2 weeks provided only a minimal further increase in the antihypertensive effect (diastolic: -10.2 mmHg; systolic: -6.7 mmHg). Diltiazem hydrochloride extended-release capsules (once-a-day dosage), given at 120 mg, 240 mg, and 480 mg/day, in a randomized, multicenter, double-blind, placebo controlled, parallel group, dose-ranging study, in 189 patients with chronic angina, demonstrated a dose-related increase in exercise time by Exercise Tolerance Test (ETT) and a reduction in rates of anginal attacks (based on individual patient diaries). The improvement in total exercise time (using the Bruce protocol), measured at trough exercise periods, for placebo, 120 mg, 240 mg, and 480 mg, was 20, 37, 49, and 56 seconds, respectively.<br/>Pharmacokinetics and Metabolism: Diltiazem is well-absorbed from the gastrointestinal tract, and is subject to an extensive first-pass effect. When given as an immediate-release oral formulation, the absolute bioavailability (compared to intravenous administration) of diltiazem is approximately 40%. Diltiazem undergoes extensive hepatic metabolism in which 2% to 4% of the unchanged drug appears in the urine. Total radioactivity measurement following short IV administration in healthy volunteers suggests the presence of other unidentified metabolites which attain higher concentrations than those of diltiazem and are more slowly eliminated; half-life of total radioactivity is about 20 hours compared to 2 to 5 hours for diltiazem. In-vitro binding studies show diltiazem is 70% to 80% bound to plasma proteins. Competitive in-vitro ligand binding studies have also shown diltiazem binding is not altered by therapeutic concentrations of digoxin, hydrochlorothiazide, phenylbutazone, propranolol, salicylic acid, or warfarin. The plasma elimination half-life of diltiazem is approximately 3.0 to 4.5 hours. Desacetyldiltiazem, the major metabolite of diltiazem, which is also present in the plasma at concentrations of 10% to20% of the parent drug, is approximately 25% to 50% as potent a coronary vasodilator as diltiazem. Therapeutic blood levels of diltiazem appear to be in the range of 40���200 ng/mL. There is a departure from linearity when dose strengths are increased; the half-life is slightly increased with dose. A study that compared patients with normal hepatic function to patients with cirrhosis found an increase in half-life and a 69% increase in bioavailability in the hepatically impaired patients. Patients with severely impaired renal function showed no difference in the pharmacokinetic profile of diltiazem compared to patients with normal renal function. Diltiazem hydrochloride extended-release capsules (once-a-day dosage) contain a controlled-release tablet formulation designed to release diltiazem over a 24-hour period. Controlled absorption of diltiazem begins within 1 hour, with maximum plasma concentrations being achieved 4 to 6 hours after administration. The apparent steady-state half-life of diltiazem following once-daily administration of diltiazem hydrochloride extended-release capsules ranges from 5 to 10 hours. This prolongation of half-life is attributed to continued absorption of diltiazem rather than to alterations in its elimination. The absolute bioavailability of diltiazem from a single dose of diltiazem hydrochloride extended-release capsules (compared to intravenous administration) is 41% (��14). This value was shown to be similar to the 40% systemic availability reported following administration of an immediate-release diltiazem hydrochloride formulation. As the dose of diltiazem hydrochloride extended-release capsules (once-a-day dosage) is increased from a daily dose of 120 mg to 240 mg, there is an increase in the AUC of 2.3 fold. When the dose is increased from 240 mg to 360 mg, AUC increases 1.6 fold and when increased from 240 mg to 480 mg, AUC increases 2.4 fold. In-vivo release of diltiazem occurs throughout the gastrointestinal tract, with controlled release still occurring for up to 24 hours after administration, as determined by radio-labeled methods. As the once-daily dose of diltiazem hydrochloride extended-release capsules was increased, departures from linearity were noted. There were disproportionate increases in area under the curve for doses from 120 mg to 480 mg. The presence of food did not affect the ability of diltiazem hydrochloride extended-release capsules to maintain a controlled release of drug and did not impact its sustained release properties over 24-hours after administration. However, simultaneous administration of diltiazem hydrochloride extended-release capsules with a high-fat breakfast resulted in increases in AUC of 13% and 19%, and in Cby 37% and 51% respectively.
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Diltiazem is contraindicated in: (1) patients with sick sinus syndrome except in the presence of a functioning ventricular pacemaker; (2) patients with second or third degree AV block except in the presence of a functioning ventricular pacemaker; (3) patients with hypotension (less than 90 mmHg systolic); (4) patients who have demonstrated hypersensitivity to the drug; and (5) patients with acute myocardial infarction and pulmonary congestion as documented by X-ray on admission.
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Diltiazem Hydrochloride Extended-release Capsules, USP (Once-a-Day Dosage) are available in 120 mg, 180 mg and 240 mg. The 120 mg capsule is a pink opaque cap/flesh opaque body, hard-shell gelatin capsule filled with two white to off-white, round, flat-faced, beveled edge tablets with no markings. The capsule is radially printed with MYLAN over 5220 in black ink on the cap. They are available as follows: NDC 0378-5220-01bottles of 100 capsulesNDC 0378-5220-05bottles of 500 capsules The 180 mg capsule is a lavender opaque cap/flesh opaque body, hard-shell gelatin capsule filled with three white to off-white, round, flat-faced, beveled edge tablets with no markings. The capsule is radially printed with MYLAN over 5280 in black ink on the cap. They are available as follows: NDC 0378-5280-01bottles of 100 capsulesNDC 0378-5280-05bottles of 500 capsules The 240 mg capsule is a light blue opaque cap/flesh opaque body, hard-shell gelatin capsule filled with four white to off-white, round, flat-faced, beveled edge tablets with no markings. The capsule is radially printed with MYLAN over 5340 in black ink on both the cap and body. They are available as follows: NDC 0378-5340-01bottles of 100 capsulesNDC 0378-5340-05bottles of 500 capsules Store at 20��to 25��C (68��to 77��F). [See USP for Controlled Room Temperature.] Dispense in a tight, light-resistant container as defined in the USP using a child-resistant closure.
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dailymed-ingredient:D&C_Red_#28_aluminum_lake,
dailymed-ingredient:D&C_Yellow_#10_aluminum_lake,
dailymed-ingredient:FD&C_Blue_#1_aluminum_lake,
dailymed-ingredient:FD&C_Blue_#2_aluminum_lake,
dailymed-ingredient:FD&C_Red_#40_aluminum_lake,
dailymed-ingredient:SDA-3A_alcohol,
dailymed-ingredient:ammonium_hydroxide,
dailymed-ingredient:colloidal_silicon_dioxide,
dailymed-ingredient:dibutyl_sebacate,
dailymed-ingredient:ethylcellulose,
dailymed-ingredient:gelatin,
dailymed-ingredient:hypromellose,
dailymed-ingredient:magnesium_stearate,
dailymed-ingredient:maltodextrin,
dailymed-ingredient:microcrystalline_cellulose,
dailymed-ingredient:n-butyl_alcohol,
dailymed-ingredient:oleic_acid,
dailymed-ingredient:pharmaceutical_glaze,
dailymed-ingredient:polyethylene_glycol,
dailymed-ingredient:propylene_glycol,
dailymed-ingredient:sodium_lauryl_sulfate,
dailymed-ingredient:synthetic_black_iron_oxide,
dailymed-ingredient:titanium_dioxide
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General: Diltiazem hydrochloride is extensively metabolized by the liver and is excreted by the kidneys and in bile. As with any drug given over prolonged periods, laboratory parameters should be monitored at regular intervals. The drug should be used with caution in patients with impaired renal or hepatic function. In subacute and chronic dog and rat studies designed to produce toxicity, high doses of diltiazem were associated with hepatic damage. In special subacute hepatic studies, oral doses of 125 mg/kg and higher in rats were associated with histological changes inthe liver which were reversible when the drug was discontinued. In dogs, doses of 20 mg/kg were also associated with hepatic changes; however, these changes were reversible with continued dosing. Dermatological events may be transient and may disappear despite continued use of diltiazem. However, skin eruptions progressing to erythema multiforme and/or exfoliative dermatitis have also been infrequently reported. Should a dermatologic reaction persist, the drug should be discontinued. Although diltiazem hydrochloride extended-release capsules (once-a-day dosage) utilize a slowly erodible matrix, caution should still be used in patients with preexisting severe gastrointestinal narrowing (pathologic or iatrogenic). There have been no reports of obstructive symptoms in patients with known strictures in association with the ingestion of diltiazem hydrochloride extended-release capsules (once-a-day dosage).<br/>Information for Patients: Diltiazem hydrochloride extended-release capsules (once-a-day dosage) should be taken on an empty stomach. Patients should be cautioned that the diltiazem hydrochloride extended-release capsules (once-a-day dosage) should not be opened, chewed or crushed, and should be swallowed whole.<br/>Drug Interactions: Due to the potential for additive effects, caution and careful titration are warranted in patients receiving diltiazem concomitantly with any agents known to affect cardiac contractility and/or conduction . Pharmacologic studies indicate that there may be additive effects in prolonging AV conduction when using beta-blockers or digitalis concomitantly with diltiazem . As with all drugs, care should be exercised when treating patients with multiple medications. Diltiazem undergoes biotransformation by cytochrome P-450 mixed function oxidase. Co-administration of diltiazem with other agents which follow the same route of biotransformation may result in the competitive inhibition of metabolism. Especially in patients with renal and/or hepatic impairment, dosages of similarly metabolized drugs, particularly those of low therapeutic ratio such as cyclosporine, may require adjustment when starting or stopping concomitantly administered diltiazem to maintain optimum therapeutic blood levels. Concomitant administration of diltiazem with carbamazepine has been reported to result in elevatedplasma levels of carbamazepine, resulting in toxicity in some cases.<br/>Beta-Blockers: Controlled and uncontrolled domestic studies suggest that concomitant use of diltiazem and beta-blockers is usually well-tolerated, but available data are not sufficient to predict the effects of concomitant treatment in patients with left ventricular dysfunction or cardiac conduction abnormalities. Administration of diltiazem concomitantly with propranolol in five normal volunteers resulted in increased propranolol levels in all subjects and the bioavailability of propranolol was increased approximately 50%. If combination therapy is initiated or withdrawn in conjunction with propranolol, an adjustment in the propranolol dose may be warranted .<br/>Cimetidine: A study in six healthy volunteers has shown a significant increase in peak diltiazem plasma levels (58%) and area-under-the-curve (53%) after a 1-week course of cimetidine at 1,200 mg per day and diltiazem 60 mg per day. Ranitidine produced smaller, nonsignificant increases. The effect may be mediated by cimetidine's known inhibition of hepatic cytochrome P-450, the enzyme system responsible for the first-pass metabolism of diltiazem. Patients currently receiving diltiazem therapy should be carefully monitored for a change in pharmacological effect when initiating and discontinuing therapy with cimetidine. An adjustment in the diltiazem dosemay be warranted.<br/>Digitalis: Administration of diltiazem with digoxin in 24 healthy male subjects increased plasma digoxin concentrations approximately 20%. Another investigator found no increase in digoxin levels in 12 patients with coronary artery disease. Since there have been conflicting results regarding the effect of digoxin levels, it is recommended that digoxin levels be monitored when initiating, adjusting, and discontinuing diltiazem therapy to avoid possible over- or under-digitalization .<br/>Anesthetics: The depression of cardiac contractility, conductivity, and automaticity as well as the vascular dilation associated with anesthetics may be potentiated by calcium channel blockers. When used concomitantly, anesthetics and calcium channel blockers should be titrated carefully.<br/>Carcinogenesis, Mutagenesis, Impairment of Fertility: A 24-month study in rats and an 18-month study in mice showed no evidence of carcinogenicity. There was also no mutagenic response in-vitro or in-vivo in mammalian cell assays or in-vitro in bacteria. No evidence of impaired fertility was observed in male or female rats at oral doses of up to 100 mg/kg/day.<br/>Pregnancy:<br/>Teratogenic Effects:<br/>Nursing Mothers: Diltiazem is excreted in human milk. One report suggests that concentrations in breast milk may approximate serum levels. If use of diltiazem is deemed essential, an alternative method of infant feeding should be instituted.<br/>Pediatric Use: Safety and effectiveness in pediatric patients have not been established.
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Diltiazem Hydrochloride
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Diltiazem Hydrochloride (Capsule, Extended Release)
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Serious adverse reactions to diltiazem hydrochloride have been rare in studies with other formulations, as well as with diltiazem hydrochloride extended-release capsules (once-a-day dosage). It should be recognized, however, that patients with impaired ventricular function and cardiac conduction abnormalities have usually been excluded from these studies.<br/>Hypertension: The most common adverse events (frequency���1%) in placebo-controlled, clinical hypertension studies with diltiazem hydrochloride extended-release capsules (once-a-day dosage) using daily doses up to 540 mg are listed in the table below with placebo-treated patients included for comparison.<br/>Angina: The most common adverse events (frequency���1%) in a placebo-controlled, short-term (2 week) clinical angina study with diltiazem hydrochloride extended-release capsules (once-a-day dosage) are listed in the table below with placebo-treated patients included for comparison. In this trial, following a placebo phase, patients were randomly assigned to once-daily doses of either 120, 240 or480 mg of diltiazem hydrochloride extended-release capsules (once-a-day dosage).<br/>Infrequent Adverse Events: The following additional events (COSTART Terms), listed by body system, were reported infrequently (less than 1%) in all subjects, hypertensive (n = 425) or angina (n = 318) patients who received diltiazem hydrochloride extended-release capsules (once-a-day dosage), or with other formulations of diltiazem.<br/>Hypertension: Cardiovascular: First-degree AV block, arrhythmia, postural hypotension, tachycardia, pallor, palpitations, phlebitis, ECG abnormality, ST elevation. Nervous System: Vertigo, hypertonia, paresthesia, dizziness, somnolence. Digestive System: Dry mouth, anorexia, tooth disorder, eructation. Skin And Appendages: Sweating, urticaria, skin hypertrophy (nevus). Respiratory System: Epistaxis, bronchitis, respiratory disorder. Urogenital System: Cystitis, kidney calculus, impotence, dysmenorrhea, vaginitis, prostate disease. Metabolic And Nutritional Disorders: Gout, edema. Musculoskeletal System: Arthralgia, bursitis, bone pain. Hemic And Lymphatic System: Lymphadenopathy. Body As A Whole: Pain, unevaluable reaction, neck pain, neck rigidity, fever, chest pain, malaise. Special Senses: Amblyopia (blurred vision), ear pain.<br/>Angina: Cardiovascular: Palpitations, AV block, sinus bradycardia, bigeminal extrasystole, angina pectoris, hypertension, hypotension, myocardial infarct, myocardial ischemia, syncope, vasodilatation, ventricular extrasystole. Nervous System: Abnormal thinking, neuropathy, paresthesia. Digestive System: Diarrhea, dyspepsia, vomiting, colitis, flatulence, GI hemorrhage, stomach ulcers. Skin And Appendages: Contact dermatitis, pruritus, sweating. Respiratory System: Respiratory distress. Urogenital System: Kidney failure, pyelonephritis, urinary tract infection. Metabolic And Nutritional Disorders: Weight increase. Musculoskeletal System: Myalgia. Body As A Whole: Chest pain, accidental injury, infection. Special Senses: Eye hemorrhage, ophthalmitis, otitis media, taste perversion, tinnitus. There have been post-marketing reports of Stevens-Johnson Syndrome and toxic epidermal necrolysis associated with the use of diltiazem.
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Cardiac Conduction: Diltiazem prolongs AV node refractory periods without significantly prolonging sinus node recovery time, except in patients with sick sinus syndrome. This effect may rarely result in abnormally slow heart rates (particularly in patients with sick sinus syndrome) or second, or third degree AV block (22 of 10,119 patients, or 0.2%); 41% of these 22 patients were receiving concomitant beta-adrenoceptor antagonists versus 17% of the total group. Concomitant use of diltiazem with beta-blockers or digitalis may result in additive effects on cardiac conduction. A patient with Prinzmetal's angina developed periods of asystole (2 to 5 seconds) after a single 60 mg dose of diltiazem.<br/>Congestive Heart Failure: Although diltiazem has a negative inotropic effect in isolated animal tissue preparations, hemodynamic studies in humans with normal ventricular function have not shown a reduction in cardiac index nor consistent negative effects on contractility (dp/dt). An acute study of oral diltiazem in patients with impaired ventricular function (ejection fraction of 24%��6%) showed improvement in indices of ventricular function without significant decrease in contractile function (dp/dt). Worsening of congestive heart failure has been reported in patients with preexisting impairment of ventricular function. Experience with the use of diltiazem in combination with beta-blockers in patients with impaired ventricular function is limited. Caution should be exercised when using this combination.<br/>Hypotension: Decreases in blood pressure associated with diltiazem therapy may occasionally result in symptomatic hypotension.<br/>Acute Hepatic Injury: Mild elevations of serum transaminases with and without concomitant elevation in alkaline phosphatase and bilirubin have been observed in clinical studies. Such elevations were usually transient and frequently resolved even with continued diltiazem treatment. In rare instances, significant elevations in alkaline phosphatase, LDH, SGOT, SGPT, and other phenomena consistent with acute hepatic injury have been noted. These reactions tended to occur early after therapy initiation (1 to 6 weeks) and have been reversible upon discontinuation of drug therapy. The relationship to diltiazem is uncertain in some cases, but probable in some others .
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Diltiazem Hydrochloride Extended-release Capsules (Once-a-Day Dosage) are indicated for the treatment of hypertension. Diltiazem hydrochloride may be used alone or in combination with other antihypertensive medications, such as diuretics. Diltiazem hydrochloride extended-release capsules (once-a-day dosage) are indicated for the management of chronic stable angina.
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| dailymed-instance:name |
Diltiazem Hydrochloride
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