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    HomeMedication GuideHydrochlorothiazide Safety
    Thiazide diuretic

    Hydrochlorothiazide: What to Know Before You Take It

    Also sold as Microzide, HydroDiuril

    What Hydrochlorothiazide Is Used For

    INDICATIONS AND USAGE Hydrochlorothiazide tablets are indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Hydrochlorothiazide has also been found useful in edema due to various forms of renal dysfunction such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. Hydrochlorothiazide tablets are 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 (see PRECAUTIONS , 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.

    Warnings

    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 (see PRECAUTIONS , Drug Interactions ). Acute Myopia and Secondary Angle-Closure Glaucoma Hydrochlorothiazide, a sulfonamide, can cause an idiosyncratic reaction, resulting in acute transient myopia and acute angle-closure glaucoma. Symptoms include acute onset of decreased visual acuity or ocular pain and typically occur within hours to weeks of drug initiation. Untreated acute angle-closure glaucoma can lead to permanent vision loss. The primary treatment is to discontinue hydrochlorothiazide as rapidly as possible. Prompt medical or surgical treatments may need to be considered if the intraocular pressure remains uncontrolled. Risk factors for developing acute angle-closure glaucoma may include a history of sulfonamide or penicillin allergy.

    Contraindications

    CONTRAINDICATIONS Anuria. Hypersensitivity to this product or to other sulfonamide-derived drugs.

    Hydrochlorothiazide Drug Interactions (4)

    Check Hydrochlorothiazide against your full medication list in our free Interaction Checker

    Most-Reported Side Effects

    Based on 206,985 reports in the FDA Adverse Event Reporting System (FAERS). Reports do not prove the drug caused the effect.

    fatigue13,580nausea13,559drug ineffective13,176diarrhoea11,582dizziness11,108headache10,609dyspnoea10,379pain10,195arthralgia8,040asthenia7,835fall7,749vomiting7,704

    Explore full Hydrochlorothiazide safety data in our free FDA Safety Explorer

    FDA Recalls (showing 12 of 20)

    Class IIOngoingJan 21, 2026

    cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.

    Recalling firm: Unichem Pharmaceuticals USA Inc.

    Class IIIOngoingNov 21, 2025

    Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe

    Recalling firm: Glenmark Pharmaceuticals Inc., USA

    Class IIOngoingJun 20, 2025

    Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.

    Recalling firm: Lupin Pharmaceuticals Inc.

    Class IIOngoingMay 7, 2024

    Presence of foreign substance: plastic-like substance.

    Recalling firm: MACLEODS PHARMA USA, INC

    Class IIITerminatedOct 20, 2023

    Failed Impurities/Degradation Specifications

    Recalling firm: Glenmark Pharmaceuticals Inc., USA

    Class IICompletedOct 5, 2022

    CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.

    Recalling firm: Aurobindo Pharma USA Inc.

    Class IITerminatedJun 29, 2022

    Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

    Recalling firm: Glenmark Pharmaceuticals Inc., USA

    Class IITerminatedJun 29, 2022

    Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

    Recalling firm: Glenmark Pharmaceuticals Inc., USA

    Class IITerminatedJun 10, 2022

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

    Recalling firm: Macleods Pharma Usa Inc

    Class IITerminatedMay 11, 2022

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .

    Recalling firm: Direct Rx

    Class IITerminatedMay 11, 2022

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .

    Recalling firm: Direct Rx

    Class IITerminatedMay 11, 2022

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .

    Recalling firm: Direct Rx

    This information is educational — not medical advice.

    This page is provided for general educational purposes and summarizes publicly available data from sources such as the U.S. Food & Drug Administration. It is not a substitute for the judgment of a licensed clinician and should not be used to start, stop, or change any medication. It may be incomplete or out of date, and individual circumstances vary. Always talk with your prescriber or pharmacist about your specific medications and health conditions. If you think you may have a medical emergency, call 911.

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