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Mega-2D

NAFDAC Reg. No. B4-2094 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 29 October 2026 · synced automatically from official sources.
Producto
Mega-2D
Número NAFDAC
B4-2094
Principio activo
Ceftriaxone (Ceftriaxone Sodium); Sulbactam (Sulbactam Sodium)
Dosis
1.5 g
Forma
Inyección
Tamaño del envase
1 x 1 vial + 10 mL sterile water for injection (in ampoule)
Fabricante
No Constan
Solicitante (titular)
Dony-Triumph and Company Nigeria Limited
Approved
15 Dec 2022
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
14 Dec 2027
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

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

Lo que encontramos

  • Mega-2D is on the NAFDAC register with an active registration (B4-2094). 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 Mega-2D

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

Before instituting treatment with Ceftriaxone for Injection, USP, appropriate specimens should be obtained for isolation of the causative organism and for determination of its susceptibility to the drug. Therapy may be instituted prior to obtaining results of susceptibility testing. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ceftriaxone for Injection, USP and other antibacterial drugs, Ceftriaxone for Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. …

Cómo tomarlo y con qué frecuencia
  • Ceftriaxone may be administered intravenously or intramuscularly
  • However, the intent of this Pharmacy Bulk Package is for the preparation of solutions for intravenous infusion only
  • Ceftriaxone should be administered intravenously by infusion over a period of 30 minutes
  • Do not use diluents containing calcium, such as Ringer ’ s solution or Hartmann ’ s solution, to reconstitute Ceftriaxone vials or to further dilute a reconstituted vial for IV administration because a precipitate can form
  • Precipitation of ceftriaxone-calcium can also occur when Ceftriaxone is mixed with calcium-containing solutions in the same IV administration line
  • Ceftriaxone must not be administered simultaneously with calcium-containing IV solutions, including continuous calcium-containing infusions such as parenteral nutrition via a Y-site
  • However, in patients other than neonates, Ceftriaxone and calcium-containing solutions may be administered sequentially of one another if the infusion lines are thoroughly flushed between infusions with a compatible fluid (see WARNINGS )
  • There have been no reports of an interaction between ceftriaxone and oral calcium-containing products or interaction between intramuscular ceftriaxone and calcium-containing products (IV or oral)
  • NEONATES: Hyperbilirubinemic
  • Neonates, especially prematures, should not be treated with Ceftriaxone
  • Ceftriaxone is contraindicated in premature
  • Neonates (see CONTRAINDICATIONS ). …
Infancia
  • Safety and effectiveness of Ceftriaxone in neonates, infants and pediatric patients have been established for the dosages described in the DOSAGE AND ADMINISTRATION section
  • In vitro studies have shown that ceftriaxone, like some other cephalosporins, can displace bilirubin from serum albumin
  • Ceftriaxone should not be administered to hyperbilirubinemic
  • Neonates, especially prematures (see CONTRAINDICATIONS )
While you are taking it
  • Patients should be counseled that antibacterial drugs including Ceftriaxone should only be used to treat bacterial infections
  • They do not treat viral infections (e.g., the common cold)
  • When Ceftriaxone 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 decrease the effectiveness of the immediate treatment and increase the likelihood that bacteria will develop resistance and will not be treatable by Ceftriaxone or other antibacterial drugs in the future. …
Talk to a doctor first if
  • Hypersensitivity Ceftriaxone is contraindicated in patients with known hypersensitivity to ceftriaxone, any of its excipients or to any other cephalosporin
  • Patients with previous hypersensitivity reactions to penicillin and other beta lactam antibacterial agents may be at greater risk of hypersensitivity to ceftriaxone (see WARNINGS – Hypersensitivity ). …
Warnings

Hypersensitivity Reactions Before therapy with Ceftriaxone is instituted, careful inquiry should be made to determine whether the patient has had previous hypersensitivity reactions to cephalosporins, penicillins and other beta-lactam agents or other drugs. This product should be given cautiously to penicillin and other beta-lactam agent-sensitive patients. Antibacterial drugs should be administered with caution to any patient who has demonstrated some form of allergy, particularly to drugs. Serious acute hypersensitivity reactions may require the use of subcutaneous epinephrine and other emergency measures. …

Posibles efectos secundarios

Ceftriaxone is generally well tolerated. In clinical trials, the following adverse reactions, which were considered to be related to Ceftriaxone therapy or of uncertain etiology, were observed: LOCAL REACTIONS - pain, induration and tenderness was 1% overall. Phlebitis was reported in

Pregnancy and breastfeeding

Pregnancy Teratogenic Effects Pregnancy Category B Reproductive studies have been performed in mice and rats at doses up to 20 times the usual human dose and have no evidence of embryotoxicity, fetotoxicity or teratogenicity. In primates, no embryotoxicity or teratogenicity was demonstrated at a dose approximately 3 times the human dose. There are, however, no adequate and well-controlled studies in pregnant women. …

If you take too much

In the case of overdosage, drug concentration would not be reduced by hemodialysis or peritoneal dialysis. There is no specific antidote. Treatment of overdosage should be symptomatic.

How to store it

Storage Prior to Reconstitution Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Protect from light.

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 2019-04-24.

Label for ceftriaxone (ceftriaxone sodium) and sulbactam (sulbactam sodium), the active ingredient registered with NAFDAC.

Check your pack of Mega-2D

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 Mega-2D

What is in Mega-2D?

Mega-2D contains Ceftriaxone (Ceftriaxone Sodium); Sulbactam (Sulbactam Sodium) (1.5 g), as injection, according to its NAFDAC registration record.

Is Mega-2D registered with NAFDAC?

Yes. Mega-2D is listed on the NAFDAC register under registration number B4-2094, and its registration is active as of 29 October 2026.

Has Mega-2D been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Mega-2D in our automatically synced alert list.

How can I check that my pack of Mega-2D is genuine?

Run a free authenticity scan with the NAFDAC number B4-2094, 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 Mega-2D?

Follow your prescription or the leaflet in your pack. The official label says: Ceftriaxone may be administered intravenously or intramuscularly. However, the intent of this Pharmacy Bulk Package is for the preparation of solutions for intravenous infusion only. Ceftriaxone should be administered intravenously by infusion over a period of 30 minutes. Do not use diluents containing calcium, such as Ringer ’ s solution or Hartmann ’ s solution, to reconstitu…

What is Mega-2D used for?

Before instituting treatment with Ceftriaxone for Injection, USP, appropriate specimens should be obtained for isolation of the causative organism and for determination of its susceptibility to the drug. Therapy may be instituted prior to obtaining results of susceptibility testing. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ceftriaxone for Injection, US (Summarised from the official U.S. FDA label for ceftriaxone (ceftriaxone sodium) and sulbactam (sulbactam sodium). Always follow your doctor or pharmacist.)

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