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Dutaz Tablet_

NAFDAC Reg. No. A4-100367 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 5 November 2026 · synced automatically from official sources.
Producto
Dutaz Tablet_
Número NAFDAC
A4-100367
Principio activo
Dutasteride
Dosis
0.5 mg
Forma
Capsule
Tamaño del envase
3 x 10's (in Alu-Alu blisters)
Fabricante
No Constan
Solicitante (titular)
Evans Medical PLC
Approved
30 Mar 2023
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
29 Mar 2028
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

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

Lo que encontramos

  • Dutaz Tablet_ is on the NAFDAC register with an active registration (A4-100367). 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 Dutaz 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.

Para quién es

Dutasteride is a 5 alpha-reductase inhibitor indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate to: (1.1) improve symptoms, reduce the risk of acute urinary retention, and reduce the risk of the need for BPH-related surgery. Dutasteride in combination with the alpha-adrenergic antagonist, tamsulosin, is indicated for the treatment of symptomatic BPH in men with an enlarged prostate. (1.2) Limitations of Use: Dutasteride is not approved for the prevention of prostate cancer. …

Cómo tomarlo y con qué frecuencia
  • The capsules should be swallowed whole and not chewed or opened, as contact with the capsule contents may result in irritation of the oropharyngeal mucosa
  • Dutasteride may be administered with or without food
  • Monotherapy: 0.5 mg once daily
  • Combination with tamsulosin: 0.5 mg once daily and tamsulosin 0.4 mg once daily
  • Dosing considerations: Swallow whole
  • May take with or without food
  • Monotherapy The recommended dose of dutasteride is 1 capsule (0.5 mg) taken once daily
  • Combination with Alpha-adrenergic Antagonist The recommended dose of dutasteride is 1 capsule (0.5 mg) taken once daily and tamsulosin 0.4 mg taken once daily
Fortalezas en las que viene

0.5 mg, yellow, oblong capsules containing clear liquid printed with ‘AT131’ with black ink. 0.5-mg capsules ( 3 )

While you are taking it
  • Advise the patient to read the FDA-approved patient labeling (Patient Information)
  • PSA Monitoring Inform patients that dutasteride reduces serum PSA levels by approximately 50% within 3 to 6 months of therapy, although it may vary for each individual
  • For patients undergoing PSA screening, increases in PSA levels while on treatment with dutasteride may signal the presence of prostate cancer and should be evaluated by a healthcare provider [see Warnings and Precautions ] . …
Talk to a doctor first if
  • Dutasteride is contraindicated for use in: Pregnancy
  • Dutasteride use is contraindicated in women who are pregnant
  • In animal reproduction and developmental toxicity studies, dutasteride inhibited development of male fetus external genitalia
  • Therefore, dutasteride may cause fetal harm when administered to a pregnant woman [see Warnings and Precautions , Use in Specific Populations ] . …
Medicines it may not mix with

Use with caution in patients taking potent, chronic cytochrome P450 (CYP)3A4 enzyme inhibitors (e.g., ritonavir). (7) 7.1 Cytochrome P450 3A Inhibitors Dutasteride is extensively metabolized in humans by the cytochrome P450 (CYP)3A4 and CYP3A5 isoenzymes. The effect of potent CYP3A4 inhibitors on dutasteride has not been studied. Because of the potential for drug-drug interactions, use caution when prescribing dutasteride to patients taking potent, chronic CYP3A4 enzyme inhibitors (e.g., ritonavir) [see Clinical Pharmacology (12.3)] . …

Warnings

Dutasteride reduces serum prostate-specific antigen (PSA) concentration by approximately 50%. However, any confirmed increase in PSA while on dutasteride may signal the presence of prostate cancer and should be evaluated, even if those values are still within the normal range for untreated men. (5.1) Dutasteride may increase the risk of high-grade prostate cancer. (5.2, 6.1) Prior to initiating treatment with dutasteride, consideration should be given to other urological conditions that may cause similar symptoms. (5.3) Women who are pregnant or may be pregnant should not handle dutasteride capsules due to potential risk to a male fetus. …

Posibles efectos secundarios

The most common adverse reactions, reported in ≥1% of subjects treated with dutasteride and more commonly than in subjects treated with placebo, are impotence, decreased libido, ejaculation disorders, and breast disorders. (6.1) To report SUSPECTED ADVERSE REACTIONS, contact Camber Pharmaceuticals, Inc., at 1-866-495-8330 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared with rates in the clinical trial of another drug and may not reflect the rates observed in practice. …

Pregnancy and breastfeeding

IN SPECIFIC POPULATIONS 8.1 Pregnancy Risk Summary Dutasteride is contraindicated for use in pregnancy because it may cause harm to the male fetus [see Contraindications (4)] . Dutasteride is not indicated for use in women. Dutasteride is a 5 alpha-reductase inhibitor that prevents conversion of testosterone to dihydrotestosterone (DHT), a hormone necessary for normal development of male genitalia. …

If you take too much

In volunteer trials, single doses of dutasteride up to 40 mg (80 times the therapeutic dose) for 7 days have been administered without significant safety concerns. In a clinical trial, daily doses of 5 mg (10 times the therapeutic dose) were administered to 60 subjects for 6 months with no additional adverse effects to those seen at therapeutic doses of 0.5 mg. There is no specific antidote for dutasteride. Therefore, in cases of suspected overdosage, symptomatic and supportive treatment should be given as appropriate, taking the long half-life of dutasteride into consideration.

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 2026-08-14.

Label for dutasteride, the active ingredient registered with NAFDAC.

Check your pack of Dutaz 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 Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Dutaz Tablet_

What is in Dutaz Tablet_?

Dutaz Tablet_ contains Dutasteride (0.5 mg), as capsule, according to its NAFDAC registration record.

Is Dutaz Tablet_ registered with NAFDAC?

Yes. Dutaz Tablet_ is listed on the NAFDAC register under registration number A4-100367, and its registration is active as of 5 November 2026.

Has Dutaz Tablet_ been flagged as fake or recalled?

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

How can I check that my pack of Dutaz Tablet_ is genuine?

Run a free authenticity scan with the NAFDAC number A4-100367, 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 Dutaz Tablet_?

Follow your prescription or the leaflet in your pack. The official label says: The capsules should be swallowed whole and not chewed or opened, as contact with the capsule contents may result in irritation of the oropharyngeal mucosa. Dutasteride may be administered with or without food. Monotherapy: 0.5 mg once daily. (2.1) Combination with tamsulosin: 0.5 mg once daily and tamsulosin 0.4 mg once daily. (2.2) Dosing considerations: Swallow whole. May tak…

What is Dutaz Tablet_ used for?

Dutasteride is a 5 alpha-reductase inhibitor indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate to: (1.1) improve symptoms, reduce the risk of acute urinary retention, and reduce the risk of the need for BPH-related surgery. Dutasteride in combination with the alpha-adrenergic antagonist, tamsulosin, is indicated for the treatment of symp (Summarised from the official U.S. FDA label for dutasteride. Always follow your doctor or pharmacist.)

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