Verifying…
Home / Drug A–Z / Bactrosec Tablet 500 mg

Bactrosec Tablet 500 mg

NAFDAC Reg. No. A4-6798 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Bactrosec Tablet 500 mg
NAFDAC number
A4-6798
Active ingredient
Secnidazole
Strength
500 mg
Form
Tablet
Pack size
1 x 4's,1 x 10's (in PVC-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
Pinnacle Health Pharmaceutical & Stores Ltd
Approved
30 Nov 2023
Status
Active View on NAFDAC ↗
Registration valid to
29 Nov 2028
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Bactrosec Tablet 500 mg is on the NAFDAC register with an active registration (A4-6798). 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.

What Bactrosec Tablet 500 mg is used for

From the official U.S. FDA label for secnidazole, the active ingredient registered with NAFDAC.

What it is used for

SOLOSEC ® is a nitroimidazole antimicrobial indicated for: Treatment of bacterial vaginosis in female patients 12 years of age and older. ( 1.1 ) Treatment of trichomoniasis in patients 12 years of age and older. ( 1.2 ) To reduce the development of drug-resistant bacteria and maintain the effectiveness of SOLOSEC and other antibacterial drugs, SOLOSEC should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. ( 1.3 ) 1.1 Bacterial Vaginosis SOLOSEC is indicated for the treatment of bacterial vaginosis in female patients 12 years of age and older [see Use in Specific Populations (8.1) and Clinical Studies (14) ]. …

Possible side effects

The following important adverse reactions are discussed in greater detail in other sections of labeling: Vulvovaginal Candidiasis [Warnings and Precautions (5.1)] Bacterial Vaginosis : Most common adverse reactions observed in clinical trials of bacterial vaginosis (incidence ≥ 2%) were vulvovaginal candidiasis, headache, nausea, dysgeusia, vomiting, diarrhea, abdominal pain, and vulvovaginal pruritus. ( 6.1 ). Trichomoniasis : Most common adverse reaction observed in the clinical trial of trichomoniasis (incidence ≥ 2%) was vulvovaginal candidiasis. ( 6.1 ). …

Do not use if

4. CONTRAINDICATIONS SOLOSEC is contraindicated: In patients who have shown hypersensitivity to secnidazole, or other nitroimidazole derivatives. In patients with Cockayne syndrome: Severe irreversible hepatotoxicity/acute liver failure with fatal outcomes have been reported after initiation of metronidazole, another nitroimidazole drug, structurally related to secnidazole, in patients with Cockayne syndrome [see Adverse Reactions (6.2) ] . …

Warnings

Vulvovaginal Candidiasis: This may develop with SOLOSEC and require treatment with an antifungal agent. ( 5.1 ) Potential Risk for Carcinogenicity : Carcinogenicity has been seen in mice and rats treated chronically with nitroimidazole derivatives, which are structurally related to secnidazole. It is unclear if the positive tumor findings in lifetime rodent studies indicate a risk to patients taking a single dose of SOLOSEC to treat bacterial vaginosis. Avoid chronic use. ( 5.2 ) 5.1 Vulvovaginal Candidiasis The use of SOLOSEC may result in vulvovaginal candidiasis. …

Pregnancy & breastfeeding

8.1 Pregnancy Risk Summary Limited available data with SOLOSEC use in pregnant women are insufficient to inform a drug associated risk of adverse developmental outcomes . In animal reproduction studies, there were no adverse developmental outcomes when secnidazole was administered orally to pregnant rats and rabbits during organogenesis at doses up to 4 times the clinical dose (see Data ). …

Storage

Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [See USP Controlled Room temperature].

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Bactrosec Tablet 500 mg

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Bactrosec Tablet 500 mg

What is in Bactrosec Tablet 500 mg?

Bactrosec Tablet 500 mg contains Secnidazole (500 mg), as tablet, according to its NAFDAC registration record.

Is Bactrosec Tablet 500 mg registered with NAFDAC?

Yes. Bactrosec Tablet 500 mg is listed on the NAFDAC register under registration number A4-6798, and its registration is active as of 27 October 2026.

Has Bactrosec Tablet 500 mg been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Bactrosec Tablet 500 mg in our automatically synced alert list.

How can I check that my pack of Bactrosec Tablet 500 mg is genuine?

Run a free authenticity scan with the NAFDAC number A4-6798, 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.

What is Bactrosec Tablet 500 mg used for?

SOLOSEC ® is a nitroimidazole antimicrobial indicated for: Treatment of bacterial vaginosis in female patients 12 years of age and older. ( 1.1 ) Treatment of trichomoniasis in patients 12 years of age and older. ( 1.2 ) To reduce the development of drug-resistant bacteria and maintain the effectiveness of SOLOSEC and other antibacterial drugs, SOLOSEC should be used only to treat or prevent infec (Summarised from the official U.S. FDA label for secnidazole. Always follow your doctor or pharmacist.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Bactrosec Tablet 500 mg? 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.