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Tramitz-H Tablet_

NAFDAC Reg. No. B4-9727 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 30 October 2026 · synced automatically from official sources.
Producto
Tramitz-H Tablet_
Número NAFDAC
B4-9727
Principio activo
Telmisartan; Hydrochlorothiazide
Dosis
40 mg; 12.5 mg
Forma
Tablet
Tamaño del envase
1 x 30's
Fabricante
No Constan
Solicitante (titular)
Leotetra Healthcare Ltd
Approved
25 Jun 2025
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
24 Jun 2030
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Telmisartan: uses, dosage and brands worldwide

Lo que encontramos

  • Tramitz-H Tablet_ is on the NAFDAC register with an active registration (B4-9727). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generado automáticamente a partir del registro NAFDAC, QUIÉN alerta y los datos de la comunidad a partir de hoy. Este no es un consejo médico. Siga siempre a su médico o farmacéutico.

How to use Tramitz-H Tablet_

Lo que dice el prospecto oficial. Si te lo recetó un médico, sigue la receta. Si el prospecto de tu caja es distinto, manda el de tu caja.

Advertencia grave: FETAL TOXICITY When pregnancy is detected, discontinue telmisartan as soon as possible [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1) ]. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1) ] WARNING: FETAL TOXICITY See full prescribing information for complete boxed warning. …
Para quién es

Telmisartan tablets, USP are an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Cardiovascular (CV) risk reduction in patients unable to take ACE inhibitors ( 1.2 ) 1.1 Hypertension Telmisartan tablets, USP are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. …

Cómo tomarlo y con qué frecuencia
  • May be administered with or without food When used for cardiovascular risk reduction, monitoring of blood pressure is recommended, and if appropriate, adjustment of medications that lower blood pressure may be necessary Indication Starting Dose Dose Range Hypertension 40 mg once daily 40 to 80 mg once daily Cardiovascular Risk Reduction 80 mg once daily 80 mg once daily Hypertension Dosage must be individualized
  • The usual starting dose of telmisartan tablets is 40 mg once a day
  • Blood pressure response is dose-related over the range of 20 to 80 mg [see Clinical Studies ]
  • Most of the antihypertensive effect is apparent within 2 weeks and maximal reduction is generally attained after 4 weeks
  • No initial dosage adjustment is necessary for elderly patients or patients with renal impairment, including those on hemodialysis
  • Patients on dialysis may develop orthostatic hypotension; their blood pressure should be closely monitored
  • Telmisartan tablets may be administered with other antihypertensive agents
  • Telmisartan tablets may be administered with or without food
  • Cardiovascular Risk Reduction The recommended dose of telmisartan tablets is 80 mg once a day and can be administered with or without food
  • It is not known whether doses lower than 80 mg of telmisartan are effective in reducing the risk of cardiovascular morbidity and mortality. …
Fortalezas en las que viene

80 mg, white to off-white, uncoated oval shaped tablets, biconvex with beveled edges, plain on one side and debossed “038” on other side. Tablets: 80mg ( 3 )

Infancia
  • Safety and effectiveness
  • In pediatric patients have not been established [see Clinical Pharmacology ]
  • Neonates with a history of in utero exposure to telmisartan If oliguria or hypotension occurs, support blood pressure and renal perfusion
  • Exchange transfusions or dialysis may be required as a means of reversing hypotension and/or substituting for disordered renal function
Older adults

Of the total number of patients receiving telmisartan in hypertension clinical studies, 551 (19%) were 65 to 74 years of age and 130 (4%) were 75 years or older. No overall differences in effectiveness and safety were observed in these patients compared to younger patients and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals c …

While you are taking it
  • Advise the patient to read the FDA-approved patient labeling (Patient Information) Pregnancy Advise female patients of childbearing age about the consequences of exposure to telmisartan during pregnancy
  • Discuss treatment options with women planning to become pregnant
  • Tell patients to report pregnancies to their physicians as soon as possible [see Warnings and Precautions and Use in Specific Populations ]
  • Lactation Advise nursing women not to breastfeed during treatment with telmisartan [see Use in Specific Populations ] . …
Talk to a doctor first if
  • Telmisartan is contraindicated in patients with known hypersensitivity (e.g., anaphylaxis or angioedema) to telmisartan or any other component of this product [see Adverse Reactions ]
  • Do not co-administer aliskiren with telmisartan in patients with diabetes. [see Drug interactions ]
  • Known hypersensitivity (e.g., anaphylaxis or angioedema) to telmisartan or any other component of this product Do not co-administer aliskiren with telmisartan in patients with diabetes
Medicines it may not mix with

Aliskiren: Do not co-administer aliskiren with telmisartan in patients with diabetes. Avoid use of aliskiren with telmisartan in patients with renal impairment (GFR

Warnings

Avoid fetal or neonatal exposure ( 5.1 ) Hypotension: Correct any volume or salt depletion before initiating therapy. Observe for signs and symptoms of hypotension ( 5.2 ) Monitor carefully in patients with impaired hepatic ( 5.4 ) or renal function ( 5.5 ) Avoid concomitant use of an ACE inhibitor and angiotensin receptor blocker ( 5.6) 5.1 Fetal Toxicity Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death. Resulting oligohydramnios can be associated with fetal lung hypoplasia and skeletal deformations. …

Posibles efectos secundarios

The following adverse reaction is described elsewhere in labeling: Renal dysfunction upon use with ramipril [see Warnings and Precautions (5.6) ] Hypertension: The most common adverse events (≥1%) reported in hypertension trials are back pain, sinusitis, and diarrhea ( 6.1 ) Cardiovascular risk reduction: The serious adverse events (≥1%) reported in cardiovascular risk reduction trials were intermittent claudication and skin ulcer ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Ascend Laboratories, LLC at 1-877-272-7901 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Telmisartan can cause fetal harm when administered to a pregnant woman. Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death (see Clinical Considerations ). …

If you take too much

Limited data are available with regard to overdosage in humans. The most likely manifestation of overdosage with telmisartan tablets would be hypotension, dizziness and tachycardia; bradycardia could occur from parasympathetic (vagal) stimulation. If symptomatic hypotension should occur, supportive treatment should be instituted. Telmisartan is not removed by hemodialysis.

Si olvidas una dosis

Tómala en cuanto te acuerdes, salvo que falte poco para la siguiente. En ese caso, sáltate la olvidada. Nunca tomes dos dosis a la vez para compensar. Revisa tu prospecto, porque algunos medicamentos son distintos.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2026-06-05.

Label for telmisartan and hydrochlorothiazide, the active ingredient registered with NAFDAC.

Check your pack of Tramitz-H Tablet_

Add the expiry date on your pack for a full Trust Score.

O haz fotos de la caja
Te quedan 3 verificaciones gratis hoy Fuentes oficiales: FDA de EE. UU. · EMA (UE) · NAFDAC · alertas de la OMS

About Tramitz-H Tablet_

What is in Tramitz-H Tablet_?

Tramitz-H Tablet_ contains Telmisartan; Hydrochlorothiazide (40 mg; 12.5 mg), as tablet, according to its NAFDAC registration record.

Is Tramitz-H Tablet_ registered with NAFDAC?

Yes. Tramitz-H Tablet_ is listed on the NAFDAC register under registration number B4-9727, and its registration is active as of 30 October 2026.

Has Tramitz-H Tablet_ been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Tramitz-H Tablet_ in our automatically synced alert list.

How can I check that my pack of Tramitz-H Tablet_ is genuine?

Run a free authenticity scan with the NAFDAC number B4-9727, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Tramitz-H Tablet_?

Follow your prescription or the leaflet in your pack. The official label says: May be administered with or without food ( 2.1 ) When used for cardiovascular risk reduction, monitoring of blood pressure is recommended, and if appropriate, adjustment of medications that lower blood pressure may be necessary ( 2.2 ) Indication Starting Dose Dose Range Hypertension ( 2.1 ) 40 mg once daily 40 to 80 mg once daily Cardiovascular Risk Reduction ( 2.2 ) 80 mg onc…

What is Tramitz-H Tablet_ used for?

Telmisartan tablets, USP are an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Cardiovascular (CV) risk reduction in patients unable to take ACE inhibitors ( 1.2 ) 1.1 Hypertension Telmisartan tablets, (Summarised from the official U.S. FDA label for telmisartan and hydrochlorothiazide. Always follow your doctor or pharmacist.)

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