Chlorothiazide (tablet)

Chlorothiazide (tablet)
Adult Indications & Dosage
Pediatric Indications & Dosage
Contraindications
Warnings & Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Administration & Monitoring
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Counseling Information
Precautions with Alcohol
Brand Names
Look-Alike Names

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Kiran Singh, M.D. [2]

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Overview

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Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

Indications

• Chlorothiazide is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy.

• Chlorothiazide has also been found useful in edema due to various forms of renal dysfunction such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure.

• Chlorothiazide is indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe forms of hypertension.

Use in Pregnancy

• Routine use of diuretics during normal pregnancy is inappropriate and exposes mother and fetus to unnecessary hazard. Diuretics do not prevent development of toxemia of pregnancy, and there is no satisfactory evidence that they are useful in the treatment of toxemia.

• Edema during pregnancy may arise from pathologic causes or from the physiologic and mechanical consequences of pregnancy. Thiazides are indicated in pregnancy when edema is due to pathologic causes, just as they are in the absence of pregnancy. Dependent edema in pregnancy, resulting from restriction of venous return by the gravid uterus, is properly treated through elevation of the lower extremities and use of support stockings. Use of diuretics to lower intravascular volume in this instance is illogical and unnecessary. During normal pregnancy there is hypervolemia which is not harmful to the fetus or the mother in the absence of cardiovascular disease. However, it may be associated with edema, rarely generalized edema. If such edema causes discomfort, increased recumbency will often provide relief. Rarely this edema may cause extreme discomfort which is not relieved by rest. In these instances, a short course of diuretic therapy may provide relief and be appropriate.

Dosage

• Therapy should be individualized according to patient response. Use the smallest dosage necessary to achieve the required response.

For Edema

• The usual adult dosage is 0.5 g to 1 g once or twice a day. Many patients with edema respond to intermittent therapy, i.e., administration on alternate days or on three to five days each week. With an intermittent schedule, excessive response and the resulting undesirable electrolyte imbalance are less likely to occur.

For Control of Hypertension

• The usual adult starting dosage is 0.5 g or 1 g a day as a single or divided dose. Dosage is increased or decreased according to blood pressure response. Rarely some patients may require up to 2 g a day in divided doses.

Off-Label Use and Dosage (Adult)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Chlorothiazide (tablet) in adult patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Chlorothiazide (tablet) in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

There is limited information regarding FDA-Labeled Use of Chlorothiazide (tablet) in pediatric patients.

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Chlorothiazide (tablet) in pediatric patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Chlorothiazide (tablet) in pediatric patients.

Contraindications

• Anuria.

• Hypersensitivity to this product or to other sulfonamide-derived drugs.

Warnings

• Use with caution in severe renal disease. In patients with renal disease, thiazides may precipitate azotemia. Cumulative effects of the drug may develop in patients with impaired renal function.

• Thiazides should be used with caution in patients with impaired hepatic function or progressive liver disease, since minor alterations of fluid and electrolyte balance may precipitate hepatic coma.

• Thiazides may add to or potentiate the action of other antihypertensive drugs.

• Sensitivity reactions may occur in patients with or without a history of allergy or bronchial asthma.

• The possibility of exacerbation or activation of systemic lupus erythematosus has been reported.

• Lithium generally should not be given with diuretics

Adverse Reactions

Clinical Trials Experience

• The following adverse reactions have been reported and, within each category, are listed in order of decreasing severity.

Body as a whole: Weakness.

• Cardiovascular: Hypotension including orthostatic hypotension (may be aggravated by alcohol, barbiturates, narcotics or antihypertensive drugs).

• Digestive: Pancreatitis, jaundice (intrahepatic cholestatic jaundice), diarrhea, vomiting, sialadenitis, cramping, constipation, gastric irritation, nausea, anorexia.

• Hematologic: Aplastic anemia, agranulocytosis, leukopenia, hemolytic anemia, thrombocytopenia.

• Hypersensitivity: Anaphylactic reactions, necrotizing angiitis (vasculitis and cutaneous vasculitis), respiratory distress including pneumonitis and pulmonary edema, photosensitivity, fever, urticaria, rash, purpura.

• Metabolic: Electrolyte imbalance, hyperglycemia, glycosuria, hyperuricemia.

• Musculoskeletal: Muscle spasm.

• Nervous System / Psychiatric: Vertigo, paresthesias, dizziness, headache, restlessness.

• Renal: Renal failure, renal dysfunction, interstitial nephritis.

• Skin: Erythema multiforme including Stevens-Johnson syndrome, exfoliative dermatitis including toxic epidermal necrolysis, alopecia.

• Special Senses: Transient blurred vision, xanthopsia.

• Urogenital: Impotence.

• Whenever adverse reactions are moderate or severe, thiazide dosage should be reduced or therapy withdrawn.

Postmarketing Experience

There is limited information regarding Postmarketing Experience of Chlorothiazide (tablet) in the drug label.

Drug Interactions

• Drug

• Description

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA):

• Pregnancy Category

Pregnancy Category (AUS):

• Australian Drug Evaluation Committee (ADEC) Pregnancy Category

There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Chlorothiazide (tablet) in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Chlorothiazide (tablet) during labor and delivery.

Nursing Mothers

There is no FDA guidance on the use of Chlorothiazide (tablet) with respect to nursing mothers.

Pediatric Use

There is no FDA guidance on the use of Chlorothiazide (tablet) with respect to pediatric patients.

Geriatic Use

There is no FDA guidance on the use of Chlorothiazide (tablet) with respect to geriatric patients.

Gender

There is no FDA guidance on the use of Chlorothiazide (tablet) with respect to specific gender populations.

Race

There is no FDA guidance on the use of Chlorothiazide (tablet) with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Chlorothiazide (tablet) in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Chlorothiazide (tablet) in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Chlorothiazide (tablet) in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Chlorothiazide (tablet) in patients who are immunocompromised.

Administration and Monitoring

Administration

• Oral

• Intravenous

Monitoring

There is limited information regarding Monitoring of Chlorothiazide (tablet) in the drug label.

• Description

IV Compatibility

There is limited information regarding IV Compatibility of Chlorothiazide (tablet) in the drug label.

Overdosage

• The most common signs and symptoms observed are those caused by electrolyte depletion (hypokalemia, hypochloremia, hyponatremia) and dehydration resulting from excessive diuresis. If digitalis has also been administered, hypokalemia may accentuate cardiac arrhythmias.

• In the event of overdosage, symptomatic and supportive measures should be employed. Emesis should be induced or gastric lavage performed. Correct dehydration, electrolyte imbalance, hepatic coma and hypotension by established procedures. If required, give oxygen or artificial respiration for respiratory impairment.

• The degree to which chlorothiazide sodium is removed by hemodialysis has not been established.

• The oral LD50 of chlorothiazide is 8.5 g/kg, greater than 10 g/kg, and greater than 1 g/kg, in the mouse, rat and dog respectively.

Pharmacology

There is limited information regarding Chlorothiazide (tablet) Pharmacology in the drug label.

Mechanism of Action

• The mechanism of the antihypertensive effect of thiazides is unknown. Chlorothiazide does not usually affect normal blood pressure.

Structure

• Chlorothiazide is a diuretic and antihypertensive. It is 6- chloro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1, 1-dioxide. Its molecular formula is C7H6CIN3O4S2 and its structural formula is:

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This image is provided by the National Library of Medicine.

• Chlorothiazide, USP is a white, or practically white crystalline compound with a molecular weight of 295.73 which is very slightly soluble in water, but readily soluble in dilute aqueous sodium hydroxide. It is soluble in urine to the extent of about 150 mg per 100 mL at pH 7.

• Each tablet for oral administration contains either 250 mg or 500 mg of chlorothiazide and the following inactive ingredients: colloidal silicon dioxide, croscarmellose sodium-Type A, magnesium stearate, microcrystalline cellulose, sodium lauryl sulfate.

Pharmacodynamics

There is limited information regarding Pharmacodynamics of Chlorothiazide (tablet) in the drug label.

Pharmacokinetics

• Chlorothiazide is not metabolized but is eliminated rapidly by the kidney. The plasma half-life of chlorothiazide is 45 to 120 minutes. After oral doses, 10 to 15 percent of the dose is excreted unchanged in the urine. Chlorothiazide crosses the placental but not the blood-brain barrier and is excreted in breast milk.

Nonclinical Toxicology

There is limited information regarding Nonclinical Toxicology of Chlorothiazide (tablet) in the drug label.

Clinical Studies

There is limited information regarding Clinical Studies of Chlorothiazide (tablet) in the drug label.

How Supplied

• Chlorothiazide tablets, USP are available containing 250 mg or 500 mg of Chlorothiazide, USP.

• The 250 mg tablets are white, round, scored tablets debossed with M to the left of the score and 50 to the right of the score on one side of the tablet and blank on the other side. They are available as follows:

• NDC 0378-0150-01

bottles of 100 tablets

• The 500 mg tablets are white, round, scored tablets debossed with MYLAN above the score and 162 below the score on one side of the tablet and blank on the other side. They are available as follows:

• NDC 0378-0162-01

bottles of 100 tablets

Storage

• Store at 20° to 25°C (68° to 77°F).
• Dispense in a tight, light-resistant container as defined in the USP using a child-resistant closure.

Images

Drug Images

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Package and Label Display Panel

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Patient Counseling Information

There is limited information regarding Patient Counseling Information of Chlorothiazide (tablet) in the drug label.

Precautions with Alcohol

• Alcohol-Chlorothiazide (tablet) interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

• CHLOROTHIAZIDE ®

Look-Alike Drug Names

• A® — B®

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.

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