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Sefzitil 500 Tablet

NAFDAC Reg. No. B4-5743 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Sefzitil 500 Tablet
NAFDAC number
B4-5743
Active ingredient
Cefuroxime (Cefuroxime Axetil)
Strength
500 mg
Form
Tablet
Manufacturer
Not listed
Applicant (holder)
Evans Baroque Limited
Approved
26 Aug 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
25 Aug 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Sefzitil 500 Tablet is on the NAFDAC register with an active registration (B4-5743). 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 Sefzitil 500 Tablet

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

Cefuroxime for Injection is indicated for the treatment of patients with infections caused by susceptible strains of the designated organisms in the following diseases: Lower Respiratory Tract Infections , including pneumonia, caused by Streptococcus pneumoniae , Haemophilus influenzae (including ampicillin-resistant strains), Klebsiella spp., Staphylococcus aureus (penicillinase- and non–penicillinase-producing strains), Streptococcus pyogenes , and Escherichia coli . Urinary Tract Infections caused by Escherichia coli and Klebsiella spp. …

How to take it and how often
  • Dosage: Adults: The usual adult dosage range for Cefuroxime for Injection is 750 mg to 1.5 grams every 8 hours, usually for 5 to 10 days
  • In uncomplicated urinary tract infections, skin and skin­-structure infections, disseminated gonococcal infections, and uncomplicated pneumonia, a 750 mg dose every 8 hours is recommended
  • In severe or complicated infections, a 1.5 gram dose every 8 hours is recommended
  • In bone and joint infections, a 1.5-gram dose every 8 hours is recommended
  • In clinical trials, surgical intervention was performed when indicated as an adjunct to therapy with Cefuroxime for Injection
  • A course of oral antibiotics was administered when appropriate following the completion of parenteral administration of Cefuroxime for Injection
  • In life-threatening infections or infections due to less susceptible organisms, 1.5 grams every 6 hours may be required
  • In bacterial meningitis, the dosage should not exceed 3 grams every 8 hours
  • The recommended dosage for uncomplicated gonococcal infection is 1.5 grams given intramuscularly as a single dose at 2 different sites together with 1 gram of oral probenecid
  • For preventive use for clean-contaminated or potentially contaminated surgical procedures, a 1.5-gram dose administered intravenously just before surgery (approximately one-half to 1 hour before the initial incision) is recommended
  • Thereafter, give 750 mg intravenously or intramuscularly every 8 hours when the procedure is prolonged. …
Children
  • Safety and effectiveness
  • Pediatric patients below 3 months of age have not been established
  • Accumulation of other members of the cephalosporin class in newborn
  • Infants (with resulting prolongation of drug half-life) has been reported
Older adults

Of the 1,914 subjects who received Cefuroxime for Injection in 24 clinical studies of cefuroxime, 901 (47%) were 65 years and older while 421 (22%) were 75 years and older. No overall differences in safety or effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater susceptibility of some older in …

While you are taking it
  • Patients should be counseled that antibacterial drugs, including Cefuroxime for Injection, should only be used to treat bacterial infections
  • They do not treat viral infections (e.g., the common cold)
  • When Cefuroxime for Injection is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed
  • Skipping doses or not completing the full course of therapy may: 1. decrease the effectiveness of the immediate treatment and, 2. …
Talk to a doctor first if

Cefuroxime is contraindicated in patients with known allergy to the cephalosporin group of antibiotics.

Medicines it may not mix with

In common with other antibiotics, cefuroxime may affect the gut flora, leading to lower estrogen reabsorption and reduced efficacy of combined estrogen/progesterone oral contraceptives.

Warnings

BEFORE THERAPY WITH CEFUROXIME FOR INJECTION IS INSTITUTED, CAREFUL INQUIRY SHOULD BE MADE TO DETERMINE WHETHER THE PATIENT HAS HAD PREVIOUS HYPERSENSITIVITY REACTIONS TO CEPHALOSPORINS, PENICILLINS, OR OTHER DRUGS. THIS PRODUCT SHOULD BE GIVEN CAUTIOUSLY TO PENICILLIN-SENSITIVE PATIENTS. ANTIBIOTICS SHOULD BE ADMINISTERED WITH CAUTION TO ANY PATIENT WHO HAS DEMONSTRATED SOME FORM OF ALLERGY, PARTICULARLY TO DRUGS. IF AN ALLERGIC REACTION TO CEFUROXIME FOR INJECTION OCCURS, DISCONTINUE THE DRUG. SERIOUS ACUTE HYPERSENSITIVITY REACTIONS MAY REQUIRE EPINEPHRINE AND OTHER EMERGENCY MEASURES. …

Possible side effects

Cefuroxime is generally well-tolerated. The most common adverse effects have been local reactions following IV administration. Other adverse reactions have been encountered only rarely. Local Reactions: Thrombophlebitis has occurred with IV administration in 1 in 60 patients. Gastrointestinal: Gastrointestinal symptoms occurred in 1 in 150 patients and included diarrhea (1 in 220 patients) and nausea (1 in 440 patients). The onset of pseudomembranous colitis may occur during or after antibacterial treatment (see WARNINGS). …

Pregnancy and breastfeeding

Pregnancy: Teratogenic Effects: Pregnancy Category B. Reproduction studies have been performed in mice at doses up to 6,400 mg/kg/day (6.3 times the recommended maximum human dose based on mg/m 2 ) and rabbits at doses up to 400 mg/kg/day (2.1 times the recommended maximum human dose based on mg/m 2 ) and have revealed no evidence of impaired fertility or harm to the fetus due to cefuroxime. …

If you take too much

Overdosage of cephalosporins can cause cerebral irritation leading to convulsions. Serum levels of cefuroxime can be reduced by hemodialysis and peritoneal dialysis.

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 2018-09-27.

Label for cefuroxime (cefuroxime axetil), the active ingredient registered with NAFDAC.

Check your pack of Sefzitil 500 Tablet

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 Sefzitil 500 Tablet

What is in Sefzitil 500 Tablet?

Sefzitil 500 Tablet contains Cefuroxime (Cefuroxime Axetil) (500 mg), as tablet, according to its NAFDAC registration record.

Is Sefzitil 500 Tablet registered with NAFDAC?

Yes. Sefzitil 500 Tablet is listed on the NAFDAC register under registration number B4-5743, and its registration is active as of 28 October 2026.

Has Sefzitil 500 Tablet been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number B4-5743, 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 Sefzitil 500 Tablet?

Follow your prescription or the leaflet in your pack. The official label says: Dosage: Adults: The usual adult dosage range for Cefuroxime for Injection is 750 mg to 1.5 grams every 8 hours, usually for 5 to 10 days. In uncomplicated urinary tract infections, skin and skin­-structure infections, disseminated gonococcal infections, and uncomplicated pneumonia, a 750 mg dose every 8 hours is recommended. In severe or complicated infections, a 1.5 gram dose …

What is Sefzitil 500 Tablet used for?

Cefuroxime for Injection is indicated for the treatment of patients with infections caused by susceptible strains of the designated organisms in the following diseases: Lower Respiratory Tract Infections , including pneumonia, caused by Streptococcus pneumoniae , Haemophilus influenzae (including ampicillin-resistant strains), Klebsiella spp., Staphylococcus aureus (penicillinase- and non–penicill (Summarised from the official U.S. FDA label for cefuroxime (cefuroxime axetil). Always follow your doctor or pharmacist.)

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