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Priorix Tetra

NAFDAC Reg. No. A6-0145 · Drug

Registered with NAFDAC. Registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Priorix Tetra
NAFDAC number
A6-0145
Active ingredient
Measles, Mumps, and Rubella (MMR); Varicella vaccine
Strength
0.5 mL
Form
Powder for injection
Pack size
0.5 mL x 1's (in vial)
Manufacturer
Not listed
Applicant (holder)
GlaxoSmithKline Consumer Nigeria PLC (GSK)
Approved
28 Feb 2024
Status
Active View on NAFDAC ↗
Registration valid to
27 Feb 2029
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Measles: uses, dosage and brands worldwide

What we found

  • Priorix Tetra is on the NAFDAC register with an active registration (A6-0145). 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 Priorix Tetra

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

Rx Only*

How to take it and how often

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Possible side effects

Symptoms persist for more than 3 days or worsen

Pregnancy and breastfeeding

If pregnant or breast-feeding ask a health professional before use

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

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 2023-11-14.

Label for measles and mumps and rubella (mmr) and varicella vaccine, the active ingredient registered with NAFDAC.

Check your pack of Priorix Tetra

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

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Priorix Tetra

What is in Priorix Tetra?

Priorix Tetra contains Measles, Mumps, and Rubella (MMR); Varicella vaccine (0.5 mL), as powder for injection, according to its NAFDAC registration record.

Is Priorix Tetra registered with NAFDAC?

Yes. Priorix Tetra is listed on the NAFDAC register under registration number A6-0145, and its registration is active as of 5 November 2026.

Has Priorix Tetra been flagged as fake or recalled?

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

How can I check that my pack of Priorix Tetra is genuine?

Run a free authenticity scan with the NAFDAC number A6-0145, 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 Priorix Tetra?

Follow your prescription or the leaflet in your pack. The official label says: Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.…

What is Priorix Tetra used for?

Rx Only* (Summarised from the official U.S. FDA label for measles and mumps and rubella (mmr) and varicella vaccine. Always follow your doctor or pharmacist.)

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