observational studies investigating the effects of Micardis
(telmisartan) compared with other treatments, including other
available ARBs, for hypertension. Note that these trials were
investigational and were conducted to expand scientific knowledge
of Micardis (telmisartan). These trials include treatment for
conditions outside of the approved indications for Micardis
(telmisartan).
*A prospective, randomised, double-blind, double-dummy,
forced-titration, multicenter, parallel group, 1-year treatment
trial to compare telMisartan 40 mg titrated to 80 mg versus
losArtan 50 mg titrated to 100 mg, in hypertensive type 2 DiabEtic
patients with Overt nephropathy.
About Micardis(R) (telmisartan) tablets
MICARDIS is an angiotensin II receptor blocker (ARB) indicated
for the treatment of hypertension and may be used alone or in
combination with other antihypertensive agents. In the clinical
trial programs PROTECTION, ONTARGET and PRoFESS, over 58,000
patients have been enrolled to investigate the cardiovascular
protective effects of MICARDIS.
For more information and full prescribing information, please
visit www.MICARDIS.com
Safety Information
USE IN PREGNANCY
When used in pregnancy during the second and third trimesters,
drugs that act directly on the renin-angiotensin system can cause
injury and even death to the developing fetus. When pregnancy is
detected, MICARDIS Tablets should be discontinued as soon as
possible (see WARNINGS, Fetal/Neonatal Morbidity and
Mortality).
MICARDIS is indicated for the treatment of hypertension.
MICARDIS is contraindicated in patients who are hypersensitive
to any of its components.
In patients with an activated renin-angiotensin system, such as
volume- and/or salt-depleted patients (e.g., those receiving high
doses of diuretics), symptomatic hypotension may occur after
initiation of MICARDIS therapy.
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