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Cika Ephedrine & Theophylline Tablet

NAFDAC Reg. No. A11-100146 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 5 November 2026 · synced automatically from official sources.
Producto
Cika Ephedrine & Theophylline Tablet
Número NAFDAC
A11-100146
Principio activo
Ephedrine Hydrochloride; Theophylline Hydrochloride
Dosis
11 mg; 120 mg
Forma
Tablet
Fabricante
No Constan
Solicitante (titular)
Michelle Laboratories Limited
Approved
24 Jun 2021
Estado
Inactive Ver en NAFDAC ↗
Registro válido hasta
23 Jun 2026
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Ephedrine hydrochloride: uses, dosage and brands worldwide

Lo que encontramos

  • Cika Ephedrine & Theophylline Tablet is on the NAFDAC register with an active registration (A11-100146). 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 Cika Ephedrine & Theophylline Tablet

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

Ephedrine sulfate injection is indicated for the treatment of clinically important hypotension occurring in the setting of anesthesia. Ephedrine sulfate injection is an alpha- and beta-adrenergic agonist and a norepinephrine-releasing agent that is indicated for the treatment of clinically important hypotension occurring in the setting of anesthesia. ( 1 )

Cómo tomarlo y con qué frecuencia
  • Should be administered by trained healthcare providers Ephedrine sulfate injection, 50 mg/mL, must be diluted before administration as an intravenous bolus dose
  • Bolus intravenous injection: 5 mg to 10 mg as needed, not to exceed 50 mg
  • General Dosage and Administration Instructions Ephedrine sulfate injection, 50 mg/mL must be diluted before administration as an intravenous bolus to achieve the desired concentration
  • Dilute with normal saline or 5% dextrose in water
  • Inspect parenteral drug products visually for particulate matter and discoloration prior to administration, whenever solution and container permit
  • Dosing
  • For the Treatment of Clinically Important Hypotension in the Setting of Anesthesia Ephedrine sulfate injection should be administered by trained healthcare providers
  • The recommended dosages
  • For the treatment of clinically important hypotension in the setting of anesthesia is an initial dose of 5 to 10 mg administered by intravenous bolus
  • Administer additional boluses as needed, not to exceed a total dosage of 50 mg
  • Adjust dosage according to the blood pressure goal (i.e., titrate to effect)
  • Prepare a 5 mg/mL Solution for Bolus Intravenous Administration For bolus intravenous administration, prepare a solution containing a final concentration of 5 mg/mL of ephedrine sulfate injection: Withdraw 50 mg (1 mL of 50 mg/mL) of ephedrine sulfate injection and dilute with 9 mL of 5% Dextrose Injection or 0.9% Sodium Chloride Injection. …
Fortalezas en las que viene

Ephedrine sulfate injection, USP is a clear, colorless, sterile solution for intravenous injection available as: single-dose 1 mL vial that contains 50 mg/mL ephedrine sulfate, equivalent to 38 mg/mL of ephedrine base Injection: 50 mg/mL ephedrine sulfate in single-dose vial ( 3 )

Infancia
  • The safety and effectiveness of ephedrine sulfate
  • In pediatric patients have not been established
  • Animal Toxicity Data In a study in which juvenile rats were administered intravenous bolus doses of 2, 10, or 60 mg/kg ephedrine sulfate daily from Postnatal Day 35 to 56, an increased incidence of mortality was noted at the high dose of 60 mg/kg
  • The no-adverse-effect level was 10 mg/kg (approximately 1.9 times a maximum daily dose of 50 mg in a 60 kg person based on body surface area)
Older adults

Clinical studies of ephedrine did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. …

Talk to a doctor first if

None None ( 4 )

Medicines it may not mix with

Interactions that Augment the Pressor Effect Oxytocin and oxytocic drugs Clinical Impact: Serious postpartum hypertension has been described in patients who received both a vasopressor (i.e., methoxamine, phenylephrine, ephedrine) and an oxytocic (i.e., methylergonovine, ergonovine). Some of these patients experienced a stroke. Intervention: Carefully monitor the blood pressure of individuals who have received both ephedrine and an oxytocic. Clonidine, propofol, monoamine oxidase inhibitors (MAOIs), atropine Clinical Impact: These drugs augment the pressor effect of ephedrine. …

Warnings

Pressor Effects with Concomitant Use with Oxytocic Drugs : Pressor effect of sympathomimetic pressor amines is potentiated ( 5.1 ) Tachyphylaxis and Tolerance : Repeated administration of ephedrine may cause tachyphylaxis ( 5.2 ) 5.1 Pressor Effect with Concomitant Oxytocic Drugs Serious postpartum hypertension has been described in patients who received both a vasopressor (i.e., methoxamine, phenylephrine, ephedrine) and an oxytocic (i.e., methylergonovine, ergonovine) [ see Drug Interactions (7) ]. Some of these patients experienced a stroke. Carefully monitor the blood pressure of individuals who have received both ephedrine and an oxytocic. …

Posibles efectos secundarios

The following adverse reactions associated with the use of ephedrine sulfate were identified in the literature. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency reliably or to establish a causal relationship to drug exposure. Gastrointestinal disorders: Nausea, vomiting Cardiac disorders: Tachycardia, palpitations (thumping heart), reactive hypertension, bradycardia, ventricular ectopics, R-R variability Nervous system disorders: Dizziness Psychiatric disorders: Restlessness Most common adverse reactions during treatment: nausea, vomiting, and tachycardia. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Available data from randomized studies, case series, and reports of ephedrine sulfate use in pregnant women have not identified a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. However, there are clinical considerations due to underlying conditions (see Clinical Considerations) . …

If you take too much

Overdose of ephedrine can cause a rapid rise in blood pressure. In the case of an overdose, careful monitoring of blood pressure is recommended. If blood pressure continues to rise to an unacceptable level, parenteral antihypertensive agents can be administered at the discretion of the clinician.

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 2023-10-30.

Label for ephedrine hydrochloride and theophylline hydrochloride, the active ingredient registered with NAFDAC.

Check your pack of Cika Ephedrine & Theophylline Tablet

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

O haz fotos de la caja
Te quedan 3 verificaciones gratis hoy Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Cika Ephedrine & Theophylline Tablet

What is in Cika Ephedrine & Theophylline Tablet?

Cika Ephedrine & Theophylline Tablet contains Ephedrine Hydrochloride; Theophylline Hydrochloride (11 mg; 120 mg), as tablet, according to its NAFDAC registration record.

Is Cika Ephedrine & Theophylline Tablet registered with NAFDAC?

Yes. Cika Ephedrine & Theophylline Tablet is listed on the NAFDAC register under registration number A11-100146, and its registration is active as of 5 November 2026.

Has Cika Ephedrine & Theophylline Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Cika Ephedrine & Theophylline Tablet in our automatically synced alert list.

How can I check that my pack of Cika Ephedrine & Theophylline Tablet is genuine?

Run a free authenticity scan with the NAFDAC number A11-100146, 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 Cika Ephedrine & Theophylline Tablet?

Follow your prescription or the leaflet in your pack. The official label says: Should be administered by trained healthcare providers ( 2.1 ) Ephedrine sulfate injection, 50 mg/mL, must be diluted before administration as an intravenous bolus dose. ( 2.1 ) Bolus intravenous injection: 5 mg to 10 mg as needed, not to exceed 50 mg. ( 2.1 ) 2.1 General Dosage and Administration Instructions Ephedrine sulfate injection, 50 mg/mL must be diluted before adminis…

What is Cika Ephedrine & Theophylline Tablet used for?

Ephedrine sulfate injection is indicated for the treatment of clinically important hypotension occurring in the setting of anesthesia. Ephedrine sulfate injection is an alpha- and beta-adrenergic agonist and a norepinephrine-releasing agent that is indicated for the treatment of clinically important hypotension occurring in the setting of anesthesia. ( 1 ) (Summarised from the official U.S. FDA label for ephedrine hydrochloride and theophylline hydrochloride. Always follow your doctor or pharmacist.)

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