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Sporfix Capsules

NAFDAC Reg. No. B4-0050 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 30 October 2026 · synced automatically from official sources.
Producto
Sporfix Capsules
Número NAFDAC
B4-0050
Principio activo
Cefixime (Cefixime Trihydrate)
Dosis
400 mg
Forma
Capsule
Tamaño del envase
1 x 10's (in AIu-AIu blister)
Fabricante
No Constan
Solicitante (titular)
Nomedi Pharmaceuticals Limited
Approved
21-Dic-2023
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
20 Dec 2028
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

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

Lo que encontramos

  • Sporfix Capsules is on the NAFDAC register with an active registration (B4-0050). 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 Sporfix Capsules

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

Cefixime for oral suspension is a cephalosporin antibacterial drug indicated in the treatment of adults and pediatric patients six months and older with the following infections: Uncomplicated Urinary Tract Infections (1.1) Otitis Media (1.2) Pharyngitis and Tonsillitis (1.3) Acute Exacerbations of Chronic Bronchitis (1.4) Uncomplicated Gonorrhea (cervical/urethral) (1.5) To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefixime for oral suspension and other antibacterial drugs, cefixime for oral suspension should be used only to treat infections that are proven or strongly suspected to be caused by bacteria. …

Cómo tomarlo y con qué frecuencia
  • Adults: 400 mg daily
  • Pediatric patients (6 months and older): 8 mg/kg/day
  • Adults The recommended dose of cefixime is 400 mg daily
  • This may be given as a 400 mg tablet or capsule daily or the 400 mg tablet may be split and given as one half tablet every 12 hours
  • For the treatment of uncomplicated cervical/urethral gonococcal infections, a single oral dose of 400 mg is recommended
  • The capsule and tablet may be administered without regard to food
  • In the treatment of infections due to Streptococcus pyogenes , a therapeutic dosage of cefixime should be administered for at least 10 days
  • Pediatric Patients (6 months or older) The recommended dose is 8 mg/kg/day of the suspension
  • This may be administered as a single daily dose or may be given in two divided doses, as 4 mg/kg every 12 hours
  • Note: A suggested dose has been determined for each pediatric weight range
  • Refer to Table 1
  • Ensure all orders that specify a dose in milliliters include a concentration, because cefixime for oral suspension is available in three different concentrations (100 mg/5 mL, 200 mg/5 mL, and 500 mg/5 mL)
  • Table 1
  • Suggested doses for pediatric patients * The preferred concentrations of oral suspension to use are 100 mg/5 mL or 200 mg/5 mL for pediatric patients in these weight ranges. …
Fortalezas en las que viene

Cefixime is available for oral administration in the following strengths: Powder for oral suspension, when reconstituted, provides either 100 mg/5 mL or 200 mg/5 mL of cefixime as trihydrate. The powder has an off-white to pale yellow color and is strawberry flavored. Oral Suspension: 100 mg/5 mL and 200 mg/5 mL (3)

Infancia
  • Safety and effectiveness of cefixime
  • In pediatric patients younger than 6 months of age have not been established
  • The incidence of gastrointestinal adverse reactions, including diarrhea and loose stools, in the pediatric patients receiving the suspension, was comparable to the incidence seen in adult patients receiving tablets
Older adults

Clinical studies did not include sufficient numbers of subjects aged 65 and older to determine whether they respond differently than younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. A pharmacokinetic study in the elderly detected differences in pharmacokinetic parameters [see Clinical Pharmacology (12.3) ] . …

While you are taking it
  • Drug Resistance Patients should be counseled that antibacterial drugs, including cefixime, should only be used to treat bacterial infections
  • They do not treat viral infections (e.g., the common cold)
  • When cefixime 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. …
Talk to a doctor first if
  • Cefixime for oral suspension is contraindicated in patients with known allergy to cefixime or other cephalosporins
  • Contraindicated in patients with known allergy to cefixime or other cephalosporins
Medicines it may not mix with

Elevated carbamazepine levels have been reported in postmarketing experience when cefixime is administered concomitantly. (7.1) Increased prothrombin time, with or without clinical bleeding, has been reported when cefixime is administered concomitantly with warfarin and anticoagulants. (7.2) 7.1 Carbamazepine Elevated carbamazepine levels have been reported in postmarketing experience when cefixime is administered concomitantly. Drug monitoring may be of assistance in detecting alterations in carbamazepine plasma concentrations. 7.2 Warfarin and Anticoagulants Increased prothrombin time, with or without clinical bleeding, has been reported when cefixime is administered concomitantly. …

Warnings

Hypersensitivity reactions including shock and fatalities have been reported with cefixime. Discontinue use if a reaction occurs. (5.1) Clostridium difficile associated diarrhea: Evaluate if diarrhea occurs. (5.2) 5.1 Hypersensitivity Reactions Anaphylactic/anaphylactoid reactions (including shock and fatalities) have been reported with the use of cefixime. Before therapy with cefixime is instituted, careful inquiry should be made to determine whether the patient has had previous hypersensitivity reactions to cephalosporins, penicillins, or other drugs. …

Posibles efectos secundarios

Most common adverse reactions are gastrointestinal such as diarrhea (16%), nausea (7%), loose stools (6%), abdominal pain (3%), dyspepsia (3%), and vomiting. (6) To report SUSPECTED ADVERSE REACTIONS, contact Aurobindo Pharma USA, Inc. at 1-866-850-2876 or FDA at 1-800-FDA-1088 or www.fda.gov/m edwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The most commonly seen adverse reactions in U.S. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Available data from published observational studies, case series, and case reports over several decades with cephalosporin use, including cefixime, in pregnant women have not established drug-associated risks of major birth defects, miscarriage, or adverse maternal or fetal outcomes (see Data) . …

If you take too much

Gastric lavage may be indicated; otherwise, no specific antidote exists. Cefixime is not removed in significant quantities from the circulation by hemodialysis or peritoneal dialysis. Adverse reactions in small numbers of healthy adult volunteers receiving single doses up to 2 g of cefixime did not differ from the profile seen in patients treated at the recommended doses.

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 2024-02-14.

Label for cefixime (cefixime trihydrate), the active ingredient registered with NAFDAC.

Check your pack of Sporfix Capsules

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 Sporfix Capsules

What is in Sporfix Capsules?

Sporfix Capsules contains Cefixime (Cefixime Trihydrate) (400 mg), as capsule, according to its NAFDAC registration record.

Is Sporfix Capsules registered with NAFDAC?

Yes. Sporfix Capsules is listed on the NAFDAC register under registration number B4-0050, and its registration is active as of 30 October 2026.

Has Sporfix Capsules been flagged as fake or recalled?

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

How can I check that my pack of Sporfix Capsules is genuine?

Run a free authenticity scan with the NAFDAC number B4-0050, 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 Sporfix Capsules?

Follow your prescription or the leaflet in your pack. The official label says: Adults: 400 mg daily (2.1) Pediatric patients (6 months and older): 8 mg/kg/day (2.2) 2.1 Adults The recommended dose of cefixime is 400 mg daily. This may be given as a 400 mg tablet or capsule daily or the 400 mg tablet may be split and given as one half tablet every 12 hours. For the treatment of uncomplicated cervical/urethral gonococcal infections, a single oral dose of 40…

What is Sporfix Capsules used for?

Cefixime for oral suspension is a cephalosporin antibacterial drug indicated in the treatment of adults and pediatric patients six months and older with the following infections: Uncomplicated Urinary Tract Infections (1.1) Otitis Media (1.2) Pharyngitis and Tonsillitis (1.3) Acute Exacerbations of Chronic Bronchitis (1.4) Uncomplicated Gonorrhea (cervical/urethral) (1.5) To reduce the development (Summarised from the official U.S. FDA label for cefixime (cefixime trihydrate). Always follow your doctor or pharmacist.)

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