Vérification…
Traduit automatiquement. Doses et mises en garde : vérifiez l'original en anglais. Lire en anglais

Fortide DPI_

NAFDAC REG NO: A4-101656 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 1 November 2026 · synced automatically from official sources.
Produit
Fortide DPI_
Numéro NAFDAC
A4-101656
Principe actif
Formoterol Fumarate Dihydrate; Budesonide
Dosage
200 mcg/Inhalation; 6 mcg/Inhalation
Forme
Inhalation powder
Conditionnement
3 x 10's (in Blisters)
Fabricant
Non répertorié
Déposant / Titulaire :
Getz Pharma Nigeria Limited
Approuvé
29 Oct 2025
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
28 Oct 2030
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Formoterol fumarate dihydrate: uses, dosage and brands worldwide

What we found

  • Fortide DPI_ is on the NAFDAC register with an active registration (A4-101656). 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.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Fortide DPI_

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Pour qui

INDICATIONS: Integra FTM is indicated for the treatment of iron deficiency anemia, and folate deficiency anemia. Integra FTM is indicated in pregnancy for the prevention and treatment of iron deficiency and to supply a maintenance dosage of folic acid.

Comment le prendre et à quelle fréquence
  • Adults (persons over 12 years of age), One capsule daily, between meals, or as prescribed by a physician
  • Do not exceed recommended dosage
  • Do not administer to children under the age of 12
Children
  • Safety and effectiveness of this product have not been established
  • In pediatric patients
Older adults

No clinical studies have been performed in patients age 65 and over to determine whether older persons respond differently from younger persons. Dosage should always begin at the low end of the dosage scale and should consider that elderly persons may have decreased hepatic, renal, or cardiac function and or concomitant diseases.

Talk to a doctor first if
  • Integra FTM is contraindicated in patients with known hypersensitivity to any of its ingredients; also, all iron compounds are contraindicated in patients with hemosiderosis, hemochromatosis, or hemolytic anemias
  • Pernicious anemia is a contraindication, as folic acid may obscure its signs and symptoms
Warnings

Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. Keep this product out of reach of children. In case of accidental overdose, call a doctor or poison control center immediately. WARNING: Folic acid alone is improper therapy in the treatment for pernicious anemia and other megaloblastic anemias where Vitamin B12 is deficient. PRECAUTIONS: General: Anemia is a manifestation that requires appropriate investigation to determine its cause or causes. No single regimen fits all cases and the status of the patient observed in follow-up is the final criterion for adequacy of therapy. …

Effets secondaires possibles

Folic Acid: Allergic sensitizations have been reported following both oral and parenteral administration of folic acid. Ferrous Fumarate: Gastrointestinal disturbances (anorexia, nausea, diarrhea, constipation, heartburn and vomiting) occur occasionally, but are usually mild and may subside with continuation of therapy. Reducing the dose and administering it with meals will minimize these effects in the sensitive patient. Increasing fiber in the diet can relieve constipation. Iron may turn stools black. This is a harmless effect that is a result of unabsorbed iron. Although the absorption of iron is best when taken between meals, giving Integra FTM after meals may control occasional G.I. …

Pregnancy and breastfeeding

USAGE IN PREGNANCY: Before Integra FTM is prescribed for megaloblastic anemia in pregnancy, appropriate diagnostic exclusion of Addisonian pernicious anemia, (due to faulty or blocked absorption of vitamin B12, or extrinsic factor or either a genetic, immunological or surgical basis) should be carried out.

If you take too much

OVERDOSE: Iron: Signs and Symptoms: Iron is toxic. Acute overdosage of iron may cause nausea and vomiting and, in severe cases, cardiovascular collapse and death. Other symptoms include pallor and cyanosis, melena, shock, drowsiness and coma. The estimated overdose of orally ingested iron is 300-mg/kg body weight. When overdoses are ingested by children, severe reactions, including fatalities, have resulted. Integra FTM should be stored beyond the reach of children to prevent against accidental iron poisoning. Keep this and all other drugs out of the reach of children. …

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

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 2022-11-08.

Label for formoterol fumarate dihydrate and budesonide, the active ingredient registered with NAFDAC.

Check your pack of Fortide DPI_

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

Ou prenez la boîte en photo
Encore 3 vérifications gratuites aujourd'hui Sources officielles : FDA américaine · EMA (UE) · NAFDAC · alertes OMS

About Fortide DPI_

What is in Fortide DPI_?

Fortide DPI_ contains Formoterol Fumarate Dihydrate; Budesonide (200 mcg/Inhalation; 6 mcg/Inhalation), as inhalation powder, according to its NAFDAC registration record.

Is Fortide DPI_ registered with NAFDAC?

Yes. Fortide DPI_ is listed on the NAFDAC register under registration number A4-101656, and its registration is active as of 1 November 2026.

Has Fortide DPI_ been flagged as fake or recalled?

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

How can I check that my pack of Fortide DPI_ is genuine?

Run a free authenticity scan with the NAFDAC number A4-101656, 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 Fortide DPI_?

Follow your prescription or the leaflet in your pack. The official label says: Adults (persons over 12 years of age), One (1) capsule daily, between meals, or as prescribed by a physician. Do not exceed recommended dosage. Do not administer to children under the age of 12.…

What is Fortide DPI_ used for?

INDICATIONS: Integra FTM is indicated for the treatment of iron deficiency anemia, and folate deficiency anemia. Integra FTM is indicated in pregnancy for the prevention and treatment of iron deficiency and to supply a maintenance dosage of folic acid. (Summarised from the official U.S. FDA label for formoterol fumarate dihydrate and budesonide. Always follow your doctor or pharmacist.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Fortide DPI_? Share your experience to help other patients. Sign in to review

Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.