Classes
DEA Class; Rx
Common Brand Names; Micardis HCT, MicardisPlus
- ARB/HCTZ Combos;
- Thiazide Combos
Description
Combination thiazide diuretic and angiotensin II antagonist
Used for hypertension
Hyperuricemia compared to diuretic monotherapy; additive efficacy; less potassium loss
Indications
Indicated for the treatment of hypertension in patients who do not respond to monotherapy.
Contraindications
Hypersensitivity (anaphylaxis, angioedema) to telmisartan, hydrochlorothiazide, or sulfonamides
Pregnancy (2nd and 3rd trimesters): Significant risk of fetal/neonatal morbidity and mortality (see Black Box Warnings)
Anuria
Do not coadminister with aliskiren in patients with diabetes
Not for initial treatment
Adverse Effects
Telmisartan
- Upper respiratory infection (7%)
- Urinary tract infection (1%)
- Back pain (3%)
- Diarrhea (3%)
- Myalgia (3%)
- Fatigue (1%)
- Sinusitis (3%)
- Peripheral edema (1%)
- Chest pain (1%)
- Hypertension (1%)
- Dyspepsia (1%)
- Headache (1%)
- Dizziness (1%)
- Pharyngitis (1%)
Hydrochlorothiazide
- Anorexia
- Epigastric distress
- Hypotension
- Orthostatic hypotension
- Photosensitivity
- Anaphylaxis
- Anemia
- Confusion
- Erythema multiforme
- Stevens-Johnson syndrome
- Exfoliative dermatitis including toxic epidermal necrolysis
- Dizziness
- Hypokalemia and/or hypomagnesemia
- Hyperuricemia
- Headache
Warnings
Acute transient myopia and acute angle-closure glaucoma has been reported, particularly with history of sulfonamide or penicillin allergy (hydrochlorothiazide is a sulfonamide)
Fixed combination product is not recommended in patients with severe renal or hepatic impairment
Dual blockade of the renin angiotensin system with ARBs, ACE inhibitors, or aliskiren associated with increased risk for renal function changes (including acute renal failure) compared to monotherapy
Electrolyte disturbances may occur
Photosensitivity may occur; instruct patients to protect skin from sun and undergo regular skin cancer screening
Hyperuricemia may occur or gout may be precipitated in certain patients receiving thiazide therapy
Hydrochlorothiazide may alter glucose tolerance and raise serum levels of cholesterol and triglycerides
Thiazides may decrease urinary calcium excretion
Caution in aortic mitral stenosis, hepatic impairment, hypercholesterolemia, hypercalcemia, parathyroid disease, pre-existing renal insufficiency, systemic lupus erythematosus, bilateral renal artery stenosis or anuria
As a consequence of inhibiting the renin-angiotensin-aldosterone system (RAA), changes in renal function may be anticipated in susceptible individuals; in patients whose renal function depends on RAA (eg, severe CHF), treatment with angiotensin-converting enzyme inhibitors and angiotensin receptor antagonists has been associated with oliguria and/or progressive azotemia and (rarely) with acute renal failure and/or death
Pregnancy and Lactation
Can cause fetal harm when administered to a pregnant woman; discontinue drug when pregnancy is dectected and treat hypertension according to guidelines during pregnancy
Because of the potential for serious adverse reactions in the breastfed infant including hypotension, hyperkalemia and renal impairment, advise a nursing woman not to breastfeed during treatment with telmisartan/amlodipine
Maximum Dosage
160 mg/day PO telmisartan and 25 mg/day PO hydrochlorothiazide.
160 mg/day PO telmisartan and 25 mg/day PO hydrochlorothiazide.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
How supplied
Telmisartan/hydrochlorothiazide
tablet
- 40mg/12.5mg
- 80mg/12.5mg
- 80mg/25mg