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Chemocef Injection

NAFDAC Reg. No. A4-6194 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 29 October 2026 · synced automatically from official sources.
Producto
Chemocef Injection
Número NAFDAC
A4-6194
Principio activo
Cefuroxime (Cefuroxime Sodium)
Dosis
750 mg
Forma
Powder for injection
Tamaño del envase
1 x 1's (in vial)
Fabricante
No Constan
Solicitante (titular)
Chez Resources Pharmaceutical Limited
Approved
3 Aug 2021
Estado
Inactive Ver en NAFDAC ↗
Registro válido hasta
2 Aug 2026
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Cefuroxime: uses, dosage and brands worldwide

Lo que encontramos

  • Chemocef Injection is on the NAFDAC register with an active registration (A4-6194). 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.

Generado automáticamente a partir del registro NAFDAC, QUIÉN alerta y los datos de la comunidad a partir de hoy. Este no es un consejo médico. Siga siempre a su médico o farmacéutico.

How to use Chemocef Injection

Lo que dice el prospecto oficial. Si te lo recetó un médico, sigue la receta. Si el prospecto de tu caja es distinto, manda el de tu caja.

Para quién es

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. …

Cómo tomarlo y con qué frecuencia
  • 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. …
Infancia
  • Safety and effectiveness
  • In 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. …

Posibles efectos secundarios

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.

Si olvidas una dosis

Tómala en cuanto te acuerdes, salvo que falte poco para la siguiente. En ese caso, sáltate la olvidada. Nunca tomes dos dosis a la vez para compensar. Revisa tu prospecto, porque algunos medicamentos son distintos.

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 sodium), the active ingredient registered with NAFDAC.

Check your pack of Chemocef Injection

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

O haz fotos de la caja
Te quedan 3 verificaciones gratis hoy Fuentes oficiales: FDA de EE. UU. · EMA (UE) · NAFDAC · alertas de la OMS

About Chemocef Injection

What is in Chemocef Injection?

Chemocef Injection contains Cefuroxime (Cefuroxime Sodium) (750 mg), as powder for injection, according to its NAFDAC registration record.

Is Chemocef Injection registered with NAFDAC?

Yes. Chemocef Injection is listed on the NAFDAC register under registration number A4-6194, and its registration is active as of 29 October 2026.

Has Chemocef Injection been flagged as fake or recalled?

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

How can I check that my pack of Chemocef Injection is genuine?

Run a free authenticity scan with the NAFDAC number A4-6194, 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 Chemocef Injection?

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 Chemocef Injection 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 sodium). Always follow your doctor or pharmacist.)

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