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Pivikto 50 mg Film Coated Tablets

NAFDAC Reg. No. A4-100496 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Pivikto 50 mg Film Coated Tablets
NAFDAC number
A4-100496
Active ingredient
Alpelisib
Strength
50 mg
Form
Tablet
Pack size
14's; 28's
Manufacturer
Not listed
Applicant (holder)
Novartis Nigeria Limited
Approved
31 Aug 2023
Status
Active View on NAFDAC ↗
Registration valid to
30 Aug 2028
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Pivikto 50 mg Film Coated Tablets is on the NAFDAC register with an active registration (A4-100496). 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 Pivikto 50 mg Film Coated Tablets

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

VIJOICE is indicated for the treatment of adult and pediatric patients 2 years of age and older with severe manifestations of PIK3CA-Related Overgrowth Spectrum (PROS) who require systemic therapy. This indication is approved under accelerated approval based on response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s). VIJOICE is a kinase inhibitor indicated for the treatment of adult and pediatric patients 2 years of age and older with severe manifestations of PIK3CA-Related Overgrowth Spectrum (PROS) who require systemic therapy. …

How to take it and how often
  • Recommended Dose: Pediatric patients (2 to less than 18 years of age): 50 mg taken orally once daily with food
  • Adult patients: 250 mg taken orally once daily with food
  • Administration: Swallow tablets whole
  • Do not chew, divide, or crush
  • For patients who cannot
  • Swallow tablets whole, use tablets or oral granules to create a suspension or a mixture
  • VIJOICE suspension made with water can be administered orally or via a nasogastric or gastric tube
  • See full prescribing information for preparation and administration instructions
  • Recommended Dosage Adult Patients The recommended dosage of VIJOICE in adult patients is 250 mg orally, once daily, administered as recommended [see Dosage and Administration ] until disease progression or unacceptable toxicity
  • Pediatric Patients (2 to less than 18 years of age) The recommended initial dosage of VIJOICE
  • Pediatric patients is 50 mg orally, once daily, administered as recommended [see Dosage and Administration ] until disease progression or unacceptable toxicity
  • Consider a dose increase to 125 mg once daily
  • Pediatric patients ≥ 6 years old for response optimization (clinical/radiological) after 24 weeks of treatment with VIJOICE at 50 mg once daily
  • When a pediatric patient turns 18 years old, consider a gradual dose increase up to 250 mg
Strengths it comes in

Tablets 50 mg: Light yellow, unscored, round and curved with beveled edges film-coated tablet, debossed with “C7” on one side and “NVR” on the other side. 125 mg: Dark yellow, unscored, ovaloid and curved with beveled edges film-coated tablet, debossed with “Y7” on one side and “NVR” on the other side. …

Children
  • The safety and effectiveness of VIJOICE have been established
  • Pediatric patients 2 to less than 18 years of age with PROS based on results from a single-arm clinical study of VIJOICE (EPIK-P1) that enrolled 39
  • Pediatric patients: 11 patients aged 2 to 5 years, 12 patients aged 6 to 11 years, and 16 patients aged 12 to less than 18 years of age [see Adverse Reactions and Clinical Studies ]
  • The safety and effectiveness of VIJOICE
  • Pediatric patients below the age of 2 years have not been established. …
Older adults

There were no adult patients aged 65 years of age or older who received VIJOICE in EPIK-P1.

While you are taking it
  • Advise the patient and their caregivers to read the FDA-approved patient labeling (Patient Information)
  • Severe Hypersensitivity Inform patients and their caregivers of the signs and symptoms of hypersensitivity
  • Advise patients and their caregivers to contact their healthcare provider immediately for signs and symptoms of hypersensitivity [see Warnings and Precautions ]
  • Severe Cutaneous Adverse Reactions Inform patients and their caregivers of the signs and symptoms of severe cutaneous adverse reactions (SCARs). …
Talk to a doctor first if
  • VIJOICE is contraindicated in patients with severe hypersensitivity to alpelisib or any of its ingredients [see Warnings and Precautions ]
  • Severe hypersensitivity to VIJOICE or to any of its ingredients
Medicines it may not mix with

CYP3A4 Inducers : Avoid coadministration of VIJOICE with a strong CYP3A4 inducer. Consider an alternative concomitant drug with no or minimal potential to induce CYP3A4. ( 7.1 ) Breast Cancer Resistance Protein (BCRP) Inhibitors : Avoid the use of BCRP inhibitors in patients treated with VIJOICE. If unable to use alternative drugs, closely monitor for increased adverse reactions. ( 7.1 ) 7.1 Effect of Other Drugs on VIJOICE CYP3A4 Inducers Avoid coadministration of VIJOICE with strong CYP3A4 inducers and consider an alternative concomitant drug with no or minimal potential to induce CYP3A4. Alpelisib is metabolized by CYP3A4. …

Warnings

Severe Hypersensitivity : Permanently discontinue VIJOICE. Promptly initiate appropriate treatment. ( 5.1 ) Severe Cutaneous Adverse Reactions (SCARs) : VIJOICE can cause SCARs, including Stevens-Johnson syndrome (SJS), erythema multiforme (EM), toxic epidermal necrolysis (TEN), and drug reaction with eosinophilia and systemic symptoms (DRESS). Interrupt VIJOICE for signs or symptoms of SCARs. Permanently discontinue VIJOICE if SCARs are confirmed. ( 2.5 , 5.2 ) Hyperglycemia : VIJOICE can cause severe hyperglycemia, in some cases associated with hyperglycemic hyperosmolar non-ketotic syndrome (HHNKS) or ketoacidosis. …

Possible side effects

The following clinically significant adverse reactions are discussed elsewhere in the labeling: Severe Hypersensitivity [see Warnings and Precautions (5.1)] Severe Cutaneous Adverse Reactions [see Warnings and Precautions (5.2)] Hyperglycemia [see Warnings and Precautions (5.3)] Pneumonitis [see Warnings and Precautions (5.4)] Diarrhea or Colitis [see Warnings and Precautions (5.5)] Most common adverse reactions (Grades 1 to 4, incidence ≥ 10%) were diarrhea, stomatitis, and hyperglycemia. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Novartis Pharmaceuticals Corporation at 1-888-669-6682 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Based on animal data and mechanism of action, VIJOICE can cause fetal harm when administered to a pregnant woman [see Clinical Pharmacology (12.1)] . There are no available data in pregnant women to inform the drug-associated risk. …

If you take too much

There is limited experience of overdose with alpelisib in clinical trials. In cases where accidental overdosage of alpelisib was reported in the clinical studies, the adverse reactions associated with the overdose were consistent with the known safety profile of alpelisib and included hyperglycemia, nausea, asthenia, and rash. Initiate general symptomatic and supportive measures in all cases of overdosage where necessary. There is no known antidote for VIJOICE.

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 2025-11-04.

Label for alpelisib, the active ingredient registered with NAFDAC.

Check your pack of Pivikto 50 mg Film Coated Tablets

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Pivikto 50 mg Film Coated Tablets

What is in Pivikto 50 mg Film Coated Tablets?

Pivikto 50 mg Film Coated Tablets contains Alpelisib (50 mg), as tablet, according to its NAFDAC registration record.

Is Pivikto 50 mg Film Coated Tablets registered with NAFDAC?

Yes. Pivikto 50 mg Film Coated Tablets is listed on the NAFDAC register under registration number A4-100496, and its registration is active as of 28 October 2026.

Has Pivikto 50 mg Film Coated Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Pivikto 50 mg Film Coated Tablets in our automatically synced alert list.

How can I check that my pack of Pivikto 50 mg Film Coated Tablets is genuine?

Run a free authenticity scan with the NAFDAC number A4-100496, 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 Pivikto 50 mg Film Coated Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Recommended Dose: Pediatric patients (2 to less than 18 years of age): 50 mg taken orally once daily with food. ( 2.1 ) Adult patients: 250 mg taken orally once daily with food. ( 2.1 ) Administration: Swallow tablets whole. Do not chew, divide, or crush. ( 2.4 ) For patients who cannot swallow tablets whole, use tablets or oral granules to create a suspension or a mixture. ( 2…

What is Pivikto 50 mg Film Coated Tablets used for?

VIJOICE is indicated for the treatment of adult and pediatric patients 2 years of age and older with severe manifestations of PIK3CA-Related Overgrowth Spectrum (PROS) who require systemic therapy. This indication is approved under accelerated approval based on response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clin (Summarised from the official U.S. FDA label for alpelisib. Always follow your doctor or pharmacist.)

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