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Inicio / Registrado en Nigeria / EM-B-PLEX Syrup## (Strength format)

EM-B-PLEX Syrup## (Strength format)

NAFDAC Reg. No. 04-0287 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 1 November 2026 · synced automatically from official sources.
Producto
EM-B-PLEX Syrup## (Strength format)
Número NAFDAC
04-0287
Principio activo
Thiamine Hydrochloride; Riboflavin; Pyridoxine Hydrochloride; Niacinamide
Dosis
see Composition
Forma
Syrup
Tamaño del envase
1 x 100 mL (in glass bottle)
Fabricante
No Constan
Solicitante (titular)
Emzor Pharmaceutical Industries Limited
Approved
28 Mar 2023
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
27 Mar 2028
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

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

Lo que encontramos

  • EM-B-PLEX Syrup## (Strength format) is on the NAFDAC register with an active registration (04-0287). 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 EM-B-PLEX Syrup## (Strength format)

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

INDICATIONS Thiamine hydrochloride injection is effective for the treatment of thiamine deficiency or beriberi whether of the dry (major symptoms related to the nervous system) or wet (major symptoms related to the cardiovascular system) variety. Thiamine hydrochloride injection should be used where rapid restoration of thiamine is necessary, as in Wernicke's encephalopathy, infantile beriberi with acute collapse, cardiovascular disease due to thiamine deficiency, or neuritis of pregnancy if vomiting is severe. It is also indicated when giving IV dextrose to individuals with marginal thiamine status to avoid precipitation of heart failure. …

Cómo tomarlo y con qué frecuencia
  • "Wet" beriberi with myocardial failure must be treated as an emergency cardiac condition, and thiamine must be administered slowly by the IV route in this situation (see WARNINGS )
  • In the treatment of beriberi, 10 to 20 mg of thiamine hydrochloride are given IM three times daily for as long as two weeks. (See WARNINGS regarding repeated injection of thiamine.) An oral therapeutic multivitamin preparation containing 5 to 10 mg thiamine, administered daily for one month, is recommended to achieve body tissue saturation
  • Infantile beriberi that is mild may respond to oral therapy, but if collapse occurs, doses of 25 mg may cautiously be given IV
  • Poor dietary habits should be corrected and an abundant and well-balanced dietary intake should be prescribed
  • Patients with neuritis of pregnancy in whom vomiting is severe enough to preclude adequate oral therapy should receive 5 to 10 mg of thiamine hydrochloride IM daily
  • In the treatment of Wernicke-Korsakoff syndrome, thiamine hydrochloride has been administered IV in an initial dose of 100 mg, followed by IM doses of 50 to 100 mg daily until the patient is consuming a regular, balanced diet. (See WARNINGS regarding repeated injections of thiamine.) Patients with marginal thiamine status to whom dextrose is being administered should receive 100 mg thiamine hydrochloride in each of the first few liters of IV fluid to avoid precipitating heart failure
  • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit
Talk to a doctor first if

CONTRINDICATIONS A history of sensitivity to thiamine or to any of the ingredients in this drug is a contraindication. (See WARNINGS for further information.)

Warnings

WARNING: This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum. Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration. …

Posibles efectos secundarios

An occasional individual may develop a hypersensitivity or life threatening anaphylactic reaction to thiamine, especially after repeated injections. Collapse and death have been reported. A feeling of warmth, pruritus, urticaria, weakness, sweating, nausea, restlessness, tightness of the throat, angioneurotic edema, cyanosis, pulmonary edema, and hemorrhage into the gastrointestinal tract have also been reported. Some tenderness and induration may follow IM use (see WARNINGS ).

If you take too much

Parenteral doses of 100 to 500 mg singly have been administered without toxic effects. However, dosages exceeding 30 mg three times a day are not utilized effectively. When the body tissues are saturated with thiamine, it is excreted in the urine as pyrimidine. As the intake of thiamine is further increased, it appears unchanged in the urine.

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 2026-05-07.

Label for thiamine hydrochloride and riboflavin and pyridoxine hydrochloride and niacinamide, the active ingredient registered with NAFDAC.

Check your pack of EM-B-PLEX Syrup## (Strength format)

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 EM-B-PLEX Syrup## (Strength format)

What is in EM-B-PLEX Syrup## (Strength format)?

EM-B-PLEX Syrup## (Strength format) contains Thiamine Hydrochloride; Riboflavin; Pyridoxine Hydrochloride; Niacinamide (see Composition), as syrup, according to its NAFDAC registration record.

Is EM-B-PLEX Syrup## (Strength format) registered with NAFDAC?

Yes. EM-B-PLEX Syrup## (Strength format) is listed on the NAFDAC register under registration number 04-0287, and its registration is active as of 1 November 2026.

Has EM-B-PLEX Syrup## (Strength format) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches EM-B-PLEX Syrup## (Strength format) in our automatically synced alert list.

How can I check that my pack of EM-B-PLEX Syrup## (Strength format) is genuine?

Run a free authenticity scan with the NAFDAC number 04-0287, 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 EM-B-PLEX Syrup## (Strength format)?

Follow your prescription or the leaflet in your pack. The official label says: "Wet" beriberi with myocardial failure must be treated as an emergency cardiac condition, and thiamine must be administered slowly by the IV route in this situation (see WARNINGS ). In the treatment of beriberi, 10 to 20 mg of thiamine hydrochloride are given IM three times daily for as long as two weeks. (See WARNINGS regarding repeated injection of thiamine.) An oral therapeu…

What is EM-B-PLEX Syrup## (Strength format) used for?

INDICATIONS Thiamine hydrochloride injection is effective for the treatment of thiamine deficiency or beriberi whether of the dry (major symptoms related to the nervous system) or wet (major symptoms related to the cardiovascular system) variety. Thiamine hydrochloride injection should be used where rapid restoration of thiamine is necessary, as in Wernicke's encephalopathy, infantile beriberi wit (Summarised from the official U.S. FDA label for thiamine hydrochloride and riboflavin and pyridoxine hydrochloride and niacinamide. Always follow your doctor or pharmacist.)

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