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| Clinical data | |
|---|---|
| Trade names | Apo-hydro, others |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a682571 |
| License data | EU EMA: by INN |
| Pregnancy category | B (D if used to treat pregnancy-induced hypertension) |
| Routes of administration | Oral (capsules, tablets, oral solution) |
| ATC code | C03AA03 ( WHO ) |
| Legal status | |
| Legal status | In general: ℞ (Prescription only) |
| Pharmacokinetic data | |
| Bioavailability | Variable (~70% on average) |
| Metabolism | Not significant [1] |
| Elimination half-life | 5.6–14.8 h |
| Excretion | Primarily kidney (>95% as unchanged drug) |
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The largest and most consistent cardiovascular outcome hydrochlorothiazide methyldopa been a reduction in the risk of stroke, but reductions hydrochlorothiazide methyldopa myocardial cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit.A total of 2271 patients hydrochlorothiazide methyldopa moderate to severe hypertension mean baseline systolic/diastolic blood pressure was 170/107 mmHg received treatments of amlodipine/valsartan/hydrochlorothiazide 10 mg/320 mg/25 mg, valsartan/hydrochlorothiazide 320 mg/25 mg, amlodipine/valsartan 10 mg/320 mg, or hydrochlorothiazide/amlodipine 25 mg/10 mg.
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