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Inicio / Registrado en Nigeria / Derm Oxytocin Injection

Derm Oxytocin Injection

NAFDAC Reg. No. C4-2001 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 6 November 2026 · synced automatically from official sources.
Producto
Derm Oxytocin Injection
Número NAFDAC
C4-2001
Principio activo
Oxytocin
Dosis
10 IU/mL
Forma
Solution for injection
Tamaño del envase
1 mL x 10's (in ampoules)
Fabricante
No Constan
Solicitante (titular)
Derm Pharmaceuticals Limited
Approved
25 Aug 2022
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
24 Aug 2027
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

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

Lo que encontramos

  • Derm Oxytocin Injection is on the NAFDAC register with an active registration (C4-2001). 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 Derm Oxytocin 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

IMPORTANT NOTICE: Oxytocin Injection, USP (synthetic) is indicated for the medical rather than the elective induction of labor. Available data and information are inadequate to define the benefits to risks considerations in the use of the drug product for elective induction. Elective induction of labor is defined as the initiation of labor for convenience in an individual with a term pregnancy who is free of medical indications. Antepartum Oxytocin injection (synthetic) is indicated for the initiation or improvement of uterine contractions, where this is desirable and considered suitable, in order to achieve early vaginal delivery for fetal or maternal reasons. …

Cómo tomarlo y con qué frecuencia
  • Dosage of oxytocin is determined by uterine response
  • The following dosage information is based upon the various regimens and indications in general use
  • Induction or Stimulation of Labor Intravenous infusion (drip method) is the only acceptable method of administration for the induction or stimulation of labor
  • Accurate control of the rate of infusion flow is essential
  • An infusion pump or other such device and frequent monitoring of strength of contractions and fetal heart rate are necessary for the safe administration of oxytocin for the induction or stimulation of labor
  • If uterine contractions become too powerful, the infusion can be abruptly stopped, and oxytocic stimulation of the uterine musculature will soon wane
  • An intravenous infusion of a non-oxytocin containing solution should be started
  • Physiologic electrolyte solutions should be used except under unusual circumstances
  • To prepare the usual solution for intravenous infusion–one mL (10 units) is combined aseptically with 1,000 mL of a non-hydrating diluent
  • The combined solution, rotated in the infusion bottle to insure thorough mixing, contains 10 mU/mL
  • Add the container with dilute oxytocic solution to the system through the use of a constant infusion pump or other such device to control accurately the rate of infusion
  • The initial dose should be no more than 1 to 2 mU/min
  • The dose may be gradually increased in increments of no more than 1 to 2 mU/min., until a contraction pattern has been established which is similar to normal labor. …
Talk to a doctor first if

Oxytocin injection (synthetic) is contraindicated in any of the following conditions: • Significant cephalopelvic disproportion; • Unfavorable fetal positions or presentations which are undeliverable without conversion prior to delivery, i.e., transverse lies; • In obstetrical emergencies where the benefit-to-risk ratio for either the fetus or the mother favors surgical intervention; • In cases of fetal distress where delivery is not imminent; • Prolonged use in uterine inertia or severe toxemia …

Warnings

Oxytocin injection (synthetic) when given for induction or stimulation of labor, must be administered only by the intravenous route and with adequate medical supervision in a hospital.

Posibles efectos secundarios

To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC at 1-800-551-7176 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. The following adverse reactions have been reported in the mother: • Anaphylactic reaction • Postpartum hemorrhage • Cardiac arrhythmia • Fatal afibrinogenemia • Nausea • Vomiting • Premature ventricular contractions • Pelvic hematoma Excessive dosage or hypersensitivity to the drug may result in uterine hypertonicity, spasm, tetanic contraction or rupture of the uterus. The possibility of increased blood loss and afibrinogenemia should be kept in mind when administering the drug. …

If you take too much

Overdosage with oxytocin injection (synthetic) depends essentially on uterine hyperactivity whether or not due to hypersensitivity to this agent. Hyperstimulation with strong (hypertonic) or prolonged (tetanic) contractions, or a resting tone of 15 to 20 mm H 2 O or more between contractions can lead to tumultuous labor, uterine rupture, cervical and vaginal lacerations, postpartum hemorrhage, uteroplacental hypoperfusion and variable deceleration of fetal heart, fetal hypoxia, hypercapnia or death. …

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 2025-03-24.

Label for oxytocin, the active ingredient registered with NAFDAC.

NAFDAC recall & alert notices

Public Alert No. 05/2026 – Alert on the Mop-up of Counterfeit Dermazin (1% Silver Sulphadiazine) Cream6 Feb 2026 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is alerting healthcare providers and the public about the circulation of counterfeit Dermazin (1% Silver Sulphadiazine) Cream.NAFDAC received a complaint from the legitimate Marketing Authorization Holder, Taylek Drugs Company Limited, concerning…Public Alert No. 005/2022- Recall of Dermaved Sensitive Cream (Unlicensed Medicine)10 Feb 2022 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control is informing healthcare providers that Medicines & Healthcare products Regulatory Agency (MHRA) in conjunction with Dermaved is recalling Dermaved Sensitive Cream due to presence of clobetasol propionate (0.001% w/w).   Clobetasol propionate is a strong…Public Alert No. 028/2020- Boots Company PLC Recalls Boots Dermacare 1% w/w Hydrocortisone Ointment, EL (20) A/47 (Batch Number: IDD) due to the presence of Pseudomonas aeruginosa12 Nov 2020 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control has been informed by the United Kingdom’s (UK) Medicine and Healthcare Product Regulatory Agency (MHRA) that Boots Company PLC has recalled Boots Dermacare 1% w/w Hydrocortisone Ointment, EL (20) A/47 (Batch Number: IDD) due to the presence of Pseudomon…

Compare the brands and batch numbers in these notices with your pack, or enter your batch number above.

Check your pack of Derm Oxytocin Injection

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

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Te quedan 3 verificaciones gratis hoy Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Derm Oxytocin Injection

What is in Derm Oxytocin Injection?

Derm Oxytocin Injection contains Oxytocin (10 IU/mL), as solution for injection, according to its NAFDAC registration record.

Is Derm Oxytocin Injection registered with NAFDAC?

Yes. Derm Oxytocin Injection is listed on the NAFDAC register under registration number C4-2001, and its registration is active as of 6 November 2026.

Has Derm Oxytocin Injection been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number C4-2001, 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 Derm Oxytocin Injection?

Follow your prescription or the leaflet in your pack. The official label says: Dosage of oxytocin is determined by uterine response. The following dosage information is based upon the various regimens and indications in general use. Induction or Stimulation of Labor Intravenous infusion (drip method) is the only acceptable method of administration for the induction or stimulation of labor. Accurate control of the rate of infusion flow is essential. An inf…

What is Derm Oxytocin Injection used for?

IMPORTANT NOTICE: Oxytocin Injection, USP (synthetic) is indicated for the medical rather than the elective induction of labor. Available data and information are inadequate to define the benefits to risks considerations in the use of the drug product for elective induction. Elective induction of labor is defined as the initiation of labor for convenience in an individual with a term pregnancy who (Summarised from the official U.S. FDA label for oxytocin. Always follow your doctor or pharmacist.)

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