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Home / Registered in Nigeria / Olithfem Loperamide Capsules Bp 2 mg

Olithfem Loperamide Capsules Bp 2 mg

NAFDAC Reg. No. A4-101073 · Drug

Registered with NAFDAC. Registration activeAs of 30 October 2026 · synced automatically from official sources.
Product
Olithfem Loperamide Capsules Bp 2 mg
NAFDAC number
A4-101073
Active ingredient
Loperamide Hydrochloride
Strength
2 mg
Form
Capsule
Pack size
10 x 1 x 10's (in PVC-AIu blisters)
Manufacturer
Not listed
Applicant (holder)
Olith Fem Pharma Ltd
Approved
22 Nov 2024
Status
Active View on NAFDAC ↗
Registration valid to
21 Nov 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Olithfem Loperamide Capsules Bp 2 mg is on the NAFDAC register with an active registration (A4-101073). 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 Olithfem Loperamide Capsules Bp 2 mg

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

Controls symptoms of diarrhea, including Travelers’ Diarrhea

How to take it and how often
  • Drink plenty of clear fluids to help prevent dehydration caused by diarrhea • find right dose on chart
  • If possible, use weight to dose; otherwise use age. • shake well before using • use only enclosed dosing cup specifically designed for use with this product
  • Do not use any other dosing device. • mL = milliliter
  • Adults and children 12 years and over 30 mL after the first loose stool; 15 mL after each subsequent loose stool; but no more than 60 mL in 24 hours
  • Children 9-11 years (60-95 lbs) 15 mL after the first loose stool; 7.5 mL after each subsequent loose stool; but no more than 45 mL in 24 hours
  • Children 6-8 years (48-59 lbs) 15 mL after the first loose stool; 7.5 mL after each subsequent loose stool; but no more than 30 mL in 24 hours
  • Children 2-5 years (34 to 47 lbs)
  • Ask a doctor
  • Children under 2 years (up to 33 lbs) do not use
While you are taking it
  • Tiredness, drowsiness or dizziness may occur
  • Be careful when driving or operating machinery
Talk to a doctor first if

• fever • mucus in the stool • a history of liver disease • a history of abnormal heart rhythm

Warnings

Allergy alert: Do not use if you have ever had a rash or other allergic reaction to loperamide HCl Heart alert: Taking more than directed can cause serious heart problems or death Do not use if you have bloody or black stool Ask a doctor before use if you have • fever • mucus in the stool • a history of liver disease • a history of abnormal heart rhythm Ask a doctor or pharmacist before use if you are taking a prescription drug. Loperamide may interact with certain prescription drugs. When using this product tiredness, drowsiness or dizziness may occur. Be careful when driving or operating machinery. …

Possible side effects

• symptoms get worse • diarrhea lasts for more than 2 days • you get abdominal swelling or bulging. These may be signs of a serious condition.

Pregnancy and breastfeeding

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

How to store it

• each 30 mL contains: sodium 15 mg • store between 20-25 ° C (68-77 ° F) Keep out of reach of children.

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 2025-04-11.

Label for loperamide hydrochloride, the active ingredient registered with NAFDAC.

Check your pack of Olithfem Loperamide Capsules Bp 2 mg

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) · NAFDAC · WHO alerts

About Olithfem Loperamide Capsules Bp 2 mg

What is in Olithfem Loperamide Capsules Bp 2 mg?

Olithfem Loperamide Capsules Bp 2 mg contains Loperamide Hydrochloride (2 mg), as capsule, according to its NAFDAC registration record.

Is Olithfem Loperamide Capsules Bp 2 mg registered with NAFDAC?

Yes. Olithfem Loperamide Capsules Bp 2 mg is listed on the NAFDAC register under registration number A4-101073, and its registration is active as of 30 October 2026.

Has Olithfem Loperamide Capsules Bp 2 mg been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Olithfem Loperamide Capsules Bp 2 mg in our automatically synced alert list.

How can I check that my pack of Olithfem Loperamide Capsules Bp 2 mg is genuine?

Run a free authenticity scan with the NAFDAC number A4-101073, 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 Olithfem Loperamide Capsules Bp 2 mg?

Follow your prescription or the leaflet in your pack. The official label says: • drink plenty of clear fluids to help prevent dehydration caused by diarrhea • find right dose on chart. If possible, use weight to dose; otherwise use age. • shake well before using • use only enclosed dosing cup specifically designed for use with this product. Do not use any other dosing device. • mL = milliliter adults and children 12 years and over 30 mL after the first lo…

What is Olithfem Loperamide Capsules Bp 2 mg used for?

controls symptoms of diarrhea, including Travelers’ Diarrhea (Summarised from the official U.S. FDA label for loperamide hydrochloride. Always follow your doctor or pharmacist.)

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