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PASURTA

ERENUMAB

FDA/BL/243-01001 ERENUMAB 70MG/ML nervous system INN generic

What it does

Erenumab is a medication used to help prevent migraines.

Commonly used for: migraines, migraine prevention

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
FDA/BL/243-01001
Registration date
2024-01-22
Expiry date
2027-02-01
Status
Valid
Active ingredient
ERENUMAB
Dosage form
ERENUMAB
Strength
70MG/ML
Pack size
-
Therapeutic class
-
ATC class (WHO)
N02CD - Calcitonin gene-related peptide (CGRP) antagonists
Drug group
NERVOUS SYSTEM
RxNorm RxCUI
2045613
Manufacturer / MAH
Amgen
Applicant / LTR
NOVARTIS PHARMA AG GHANA
Country of origin
-
Manufacturer location
Juncos, 00777, Puerto Rico

Source: Food and Drugs Authority · fetched 2026-04-18 08:33:04 · updated 2026-09-18 04:00:07

Disclaimer: This information is sourced from Food and Drugs Authority (Ghana). Always consult a qualified healthcare professional before using any medication.

About this medicine

Erenumab is a medication used to help prevent migraines.

What it treats

  • migraines
  • migraine prevention

How it works

Erenumab works by blocking a specific protein involved in the development of migraines, helping to reduce the frequency and severity of migraine attacks.

Who it's for

This medication is for adults who experience frequent migraines and want to reduce the number of migraine days.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: Erenumab

BNF-referenced

Erenumab is a human monoclonal antibody designed for the prophylaxis of migraine. It acts by binding to the calcitonin gene-related peptide (CGRP) receptor, thus inhibiting the function of CGRP, a key molecule involved in migraine pathophysiology. This drug is indicated for patients experiencing frequent migraine attacks and is typically initiated by a specialist.

Indications

  • Prophylaxis of migraine in adults with a history of frequent migraine attacks

Dosage

Children: Refer to the BNF for Children for pediatric dosing information.

Adults: Initially, 100 mg subcutaneously every 12 weeks; may increase to 300 mg every 12 weeks if necessary, with assessment for dose escalation within the first 12 weeks.

Mechanism of action

Erenumab binds specifically to the calcitonin gene-related peptide (CGRP) receptor, inhibiting its activity. This blockade prevents the physiological effects of CGRP, which include vasodilation and inflammation associated with migraine attacks.

Pharmacodynamics

By inhibiting the action of CGRP, Erenumab reduces the frequency and severity of migraine attacks. Clinical studies have demonstrated its efficacy in decreasing the number of migraine days experienced by patients, with a favorable safety profile.

Pharmacokinetics

Erenumab is administered via subcutaneous injection and has a half-life that allows for dosing every 12 weeks. It demonstrates linear pharmacokinetics with minimal variability among patients. The drug is primarily eliminated through the reticuloendothelial system, and its clearance may be influenced by factors such as body weight.

Contra-indications

  • Hypersensitivity to the active substance or to any of the excipients
  • Severe hepatic impairment

Adverse effects

  • Fatigue
  • Hypersensitivity reactions
  • Nasopharyngitis

Interactions

  • No significant drug interactions documented; however, caution is advised when used with other medications affecting migraine management

Precautions

  • Use with caution in patients with mild to moderate hepatic impairment
  • Monitor patients for signs of hypersensitivity reactions
  • Review treatment after 6 months of therapy

Pregnancy

Avoid use during pregnancy due to limited information available regarding safety.

Breast-feeding

Amount too small to be harmful; use with caution during breastfeeding.

Storage

Store in a refrigerator at 2-8°C, protect from light.

Formulations

  • Solution for infusion
BNF 85 (British National Formulary) p.534 PubChem / pathway

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.