Drug profile
Hydrochlorothiazide
Adult, child, renal, hepatic, pregnancy and breastfeeding information, with the source named on every line.
DRUG INFORMATION
ADULT
- Adults: For Edema: The usual adult dosage is 25 mg to 100 mg daily as a single or
divided dose.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'dosage and administration', retrieved 2026-08-29
- For Control of Hypertension: The usual initial dose in adults is 25 mg daily given
as a single dose.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'dosage and administration', retrieved 2026-08-29
- The dose may be increased to 50 mg daily, given as a single or two divided doses.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'dosage and administration', retrieved 2026-08-29
CHILD
- There are no well-controlled clinical trials in pediatric patients. Information on
dosing in this age group is supported by evidence from empiric use in pediatric
patients and published literature regarding the treatment of hypertension in such
patients. (See DOSAGE AND ADMINISTRATION: Infants and Children ).
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'pediatric use', retrieved 2026-08-29
- Therapy should be individualized according to patient response. Use the smallest
dosage necessary to achieve the required response. Adults: For Edema: The usual
adult dosage is 25 mg to 100 mg daily as a single or divided dose. Many patients
with edema respond to intermittent therapy, i.e., administration on alternate days
or on three to five days each week.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'dosage and administration', retrieved 2026-08-29
- Infants and Children: For Diuresis and For Control of Hypertension: The usual
pediatric dosage is 0.5 to 1 mg per pound (1 to 2 mg/kg) per day in single or two
divided doses, not to exceed 37.5 mg per day in infants up to 2 years of age or
100 mg per day in children 2 to 12 years of age.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'dosage and administration', retrieved 2026-08-29
RENAL IMPAIRMENT
- No kidney-impairment dose in this label. Not a statement that none is needed.
Source: Read and found silent: the US FDA label for hydrochlorothiazide
(Hydrochlorothiazide), retrieved 2026-08-29
HEPATIC IMPAIRMENT
- No liver-impairment dose in this label. Not a statement that none is needed.
Source: Read and found silent: the US FDA label for hydrochlorothiazide
(Hydrochlorothiazide), retrieved 2026-08-29
PREGNANCY [ CAUTION ]
The label allows it only when the benefit is judged to outweigh the risk. Read the
quote below.
- Pregnancy Category B Studies in which hydrochlorothiazide was orally administered
to pregnant mice and rats during their respective periods of major organogenesis
at doses up to 3000 and 1000 mg hydrochlorothiazide/kg, respectively, provided no
evidence of harm to the fetus.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'pregnancy', retrieved 2026-08-29
- There are, however, no adequate and well-controlled studies in pregnant women.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'pregnancy', retrieved 2026-08-29
- Because animal reproduction studies are not always predictive of human response,
this drug should be used during pregnancy only if clearly needed.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'pregnancy', retrieved 2026-08-29
BREASTFEEDING
- Because of the potential for serious adverse reactions in nursing infants, a
decision should be made whether to discontinue nursing or to discontinue
hydrochlorothiazide, taking into account the importance of the drug to the mother.
Source: US FDA label for hydrochlorothiazide (Hydrochlorothiazide), section
'nursing mothers', retrieved 2026-08-29