Buy Micardis
Micardis

0.89
A long-acting blood pressure medication used to prevent strokes, heart attacks, and kidney problems.


Ingredient
Availability
In Stock
Delivery
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Alternative/Local Brand
Micardis
Active Ingredient(s)
Telmisartan
Primary Category
Blood Pressure Control
Therapeutic Class
Angiotensin II Receptor Blockers (ARBs)
Pharmacological Class
Antihypertensives
Indications
Hypertension (high blood pressure), Reduction of cardiovascular risk
Contraindications
Second and third trimester of pregnancy, Biliary obstructive disorders, Severe liver impairment
Minor Side Effects
Fatigue, Nasal congestion, Mild dizziness
Moderate Side Effects
Back pain, Diarrhoea, Flu-like symptoms
Serious Side Effects
Kidney dysfunction, High potassium levels, Leg cramps, Shortness of breath
Dosage Forms
Tablet
Administration Route
Oral
Mechanism of Action
Telmisartan blocks the action of a natural substance called angiotensin II, which causes blood vessels to tighten. By blocking this, the medication allows blood vessels to relax and widen, which lowers blood pressure and improves blood flow.
Prescription Status
Rx
Manufacturer
Boehringer Ingelheim
Patient Summary
A long-acting blood pressure medication used to prevent strokes, heart attacks, and kidney problems.
Onset Time
Within 3 hours
Duration
24 hours
Storage Instructions
Store in original package to protect from moisture.
Drug Interactions
Digoxin, Lithium, Potassium supplements, NSAIDs
Age Restrictions
Safety not established in children
Pregnancy Use
Must be avoided; contact doctor if pregnancy occurs.
Alternative Drugs
Losartan, Candesartan

What is Micardis?

Micardis is a prescription-only pill that contains the active ingredient telmisartan. Telmisartan belongs to the class of drugs known as angiotensin II receptor blockers (ARBs) and is used to treat conditions related to high blood pressure and certain heart-related disorders. In Hong Kong, Micardis is regulated by the Pharmacy and Poisons Board and is available in three strengths: 20 mg, 40 mg, and 80 mg tablets.

How Micardis Works in the Body

Telmisartan blocks the binding of angiotensin II to the AT-1 receptors found on blood vessels and the adrenal gland. By preventing this interaction, the drug:

  • Relaxes the smooth muscle of blood vessels, leading to vasodilation and lower arterial pressure.
  • Reduces the release of aldosterone, which decreases sodium and water retention.
  • Slows the progression of vascular remodeling that contributes to heart disease.

The onset of blood-pressure reduction usually occurs within a few hours, with peak effect reached after about 24 hours. Telmisartan has a long half-life (≈24 hours), allowing once-daily dosing.

Conditions Treated by Micardis

Micardis is FDA- and EMA-approved for the following indications, which also apply under Hong Kong regulatory guidance:

  • Essential (primary) hypertension - to lower systolic and diastolic blood pressure.
  • Reduction of cardiovascular risk in patients with documented left-ventricular hypertrophy, diabetes, or high cardiovascular risk, when used alone or with other antihypertensives.

These uses target adult patients; the medication is not intended for children or adolescents without a specific clinician order.

Evidence-Based Off-Label Uses

Diabetic Nephropathy

Clinical studies have shown that telmisartan can slow the decline of kidney function in patients with type 2 diabetes and micro-albuminuria. This use is not approved by the Hong Kong Department of Health and should only be considered under close medical supervision.

Off-label use requires individualized risk assessment and ongoing monitoring by a qualified healthcare professional.

Who Should (Not) Use Micardis?

Absolute Contraindications

  • Known hypersensitivity to telmisartan or any tablet excipient.
  • Pregnancy (especially second and third trimesters) or lactation - ARBs can cause fetal renal damage.
  • Severe hepatic impairment (Child-Pugh C) - drug clearance is markedly reduced.

Relative Contraindications & Precautions

  • Moderate to severe renal impairment (creatinine clearance <30 mL/min). Dose reduction may be needed.
  • Hyperkalemia or use of potassium-sparing diuretics/supplements.
  • Concomitant use of ACE inhibitors or other ARBs - increased risk of hypotension and hyperkalemia.
  • Elderly patients - may be more sensitive to blood-pressure lowering effects; start with the lowest dose (20 mg).

Special Populations

  • Pregnancy: Discontinue immediately if pregnancy is detected.
  • Breastfeeding: Avoid use; telmisartan is excreted in milk.
  • Geriatric: Consider starting at 20 mg and monitor renal function.

If any of the above conditions apply, discuss alternatives with a healthcare provider.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Dizziness or light-headedness (especially after the first dose).
  • Headache.
  • Fatigue or tiredness.
  • Upper respiratory symptoms such as nasal congestion.

These effects are usually mild and transient; they often improve with continued therapy.

Serious Adverse Events

  • Angioedema - swelling of the face, lips, tongue, or airway; seek emergency care.
  • Severe hypotension - marked drop in blood pressure causing fainting.
  • Renal function deterioration - indicated by rising serum creatinine.
  • Hyperkalemia - elevated potassium levels that can precipitate cardiac arrhythmias.

Black-box warnings for ARBs focus on fetal toxicity and the risk of angioedema.

Drug Interactions

  • Potassium-containing products (potassium supplements, salt substitutes) - may raise serum potassium.
  • Concomitant ACE inhibitors or other ARBs - increase risk of hypotension, hyperkalemia, and renal impairment.
  • Non-steroidal anti-inflammatory drugs (NSAIDs) - can blunt antihypertensive effect and worsen renal function.
  • Lithium - ARBs may raise lithium concentrations; monitor plasma levels.
  • Cyclosporine - may increase the risk of nephrotoxicity.

Food and Lifestyle Interactions

  • Micardis can be taken with or without food; food does not significantly affect absorption.
  • Alcohol does not interact directly but may augment hypotensive effects.
  • Patients should avoid sudden changes in posture (e.g., standing up quickly) to reduce dizziness.

How to Take Micardis

  • Standard adult dosing:

  • Start with 40 mg once daily.

  • If needed, the dose may be increased to 80 mg once daily based on blood-pressure response.

  • For patients with renal impairment or the elderly, begin with 20 mg once daily and titrate cautiously.

  • Administration: Swallow the tablet whole with a glass of water. Do not crush or chew unless a specific preparation is advised by a pharmacist.

  • Missed dose: Take the missed tablet as soon as remembered on the same day; if it is almost time for the next dose, skip the missed one and continue the regular schedule. Do not double-dose.

  • Overdose: Symptoms may include severe hypotension, rapid heartbeat, and dizziness. Seek immediate medical attention; treatment is supportive (e.g., intravenous fluids, vasopressors). No specific antidote is available.

  • Discontinuation: Gradual tapering is not required for telmisartan, but stopping abruptly may cause rebound hypertension in some patients. Follow up with a clinician for a safe cessation plan.

Monitoring and Follow-Up

  • Blood pressure: Check at baseline, after 2-4 weeks of therapy, and periodically thereafter.
  • Renal function: Serum creatinine and estimated glomerular filtration rate (eGFR) should be measured before initiation and at 1-2 months after dose changes.
  • Electrolytes: Serum potassium should be monitored, especially when combined with potassium-sparing agents or in patients with renal disease.
  • Liver function: Routine monitoring is not mandatory but may be considered in patients with pre-existing hepatic disease.

Regular follow-up visits allow dose adjustments and early detection of adverse events.

Storage and Handling

  • Store Micardis tablets at room temperature (15 °C-30 °C), away from excess moisture and direct sunlight.
  • Keep the container tightly closed and out of reach of children.
  • Do not use tablets after the printed expiration date.
  • For disposal, follow local pharmacy-take-back programs or municipal hazardous-waste guidelines.

Medication-Specific Glossary

Angiotensin II Receptor Blocker (ARB)
A drug class that inhibits the action of angiotensin II at AT-1 receptors, producing vasodilation and reduced blood pressure.
Hyperkalemia
An abnormally high level of potassium in the blood, which can affect cardiac rhythm.
Renin-Angiotensin System (RAS)
A hormonal cascade that regulates blood pressure, fluid balance, and electrolyte homeostasis; ARBs act within this system.

Medical Disclaimer

This article provides educational information about Micardis and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Micardis FAQ

Can Micardis be taken with other blood-pressure medicines?

Yes, Micardis can be combined with other antihypertensives such as thiazide diuretics or calcium-channel blockers to achieve better blood-pressure control. However, concurrent use with other ARBs or ACE inhibitors is generally avoided due to the increased risk of hyperkalemia and renal impairment.

What does the Micardis tablet look like?

In Hong Kong the 20 mg, 40 mg, and 80 mg tablets have distinct colors and imprint codes that help differentiate strengths. For example, 20 mg tablets may be white with a specific imprint, while 80 mg tablets are often pink with a different code. Always verify the imprint against the pharmacy label.

Will Micardis show up on a drug test for employment?

Micardis is not a controlled substance and is not screened for in standard workplace drug-testing panels. It will only be detected if a specific test for ARBs is ordered, which is uncommon.

Is it safe to travel internationally with Micardis?

Yes, but carry the medication in its original labeled container and bring a copy of the prescription. Some countries require documentation for prescription medicines; having a doctor’s note in English can facilitate customs clearance.

Can I switch from a different ARB to Micardis without a wash-out period?

Transitioning between ARBs is generally safe, but a brief overlap is unnecessary. Your healthcare provider may advise a direct switch, monitoring blood pressure and renal function during the first few weeks.

How does Micardis compare with other ARBs like losartan?

Both drugs block the same receptor, but telmisartan has a longer half-life, allowing once-daily dosing without the need for multiple doses. Some studies suggest telmisartan may offer modest additional benefits in metabolic parameters, though clinical outcomes are comparable.

Are there any diet restrictions while taking Micardis?

No special dietary restrictions are required. However, maintaining a consistent sodium intake supports optimal blood-pressure control, and excessive salty foods can counteract the drug’s effect.

What should I do if I miss a dose while on a weekend?

Take the missed tablet as soon as you remember on the same day, unless it is close to the time of your next scheduled dose. In that case, skip the missed dose and resume your regular dosing schedule. Do not double the dose to catch up.

How long does a Micardis tablet remain stable after opening the bottle?

The tablets remain stable for the duration of the labeled expiration date when stored properly. Exposure to high humidity or heat can degrade the product faster, so keep the bottle tightly closed in a dry environment.

Why are generic versions of telmisartan sometimes cheaper in Hong Kong?

Generic telmisartan formulations are produced by multiple manufacturers after patent expiry, leading to market competition and lower prices. The active ingredient is identical, but inactive excipients may differ slightly; efficacy and safety remain comparable under regulatory approval.

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