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Midashin 5 mg/mL Injection

NAFDAC REG NO: A4-101180 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 4 November 2026 · synced automatically from official sources.
Controlled medicine: MidazolamPrescription only. A licensed pharmacist may sell it only against a doctor's prescription.

Midazolam · Benzodiazepine (sedative) · UN 1971 Schedule IV

  • Dependence after a few weeks of daily use; do not stop suddenly
  • Drowsiness, falls and road accidents
  • Dangerous with alcohol or opioid painkillers: breathing can stop
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Produit
Midashin 5 mg/mL Injection
Numéro NAFDAC
A4-101180
Principe actif
Midazolam (Midazolam Hydrochloride)
Dosage
5 mg/mL
Forme
Injection
Conditionnement
2 x 5's x 3 mL (in amber bottles)
Fabricant
Non répertorié
Déposant / Titulaire :
Shinfield Pharmaceuticals Limited
Approuvé
30 Jan 2025
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
29 Jan 2030
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Midazolam: uses, dosage and brands worldwide

What we found

  • Midashin 5 mg/mL Injection is on the NAFDAC register with an active registration (A4-101180). 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.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Midashin 5 mg/mL Injection

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Mise en garde grave : WARNINGS Personnel and Equipment for Monitoring and Resuscitation Adults and Pediatrics: Intravenous midazolam has been associated with respiratory depression and respiratory arrest, especially when used for sedation in noncritical care settings. In some cases, where this was not recognized promptly and treated effectively, death or hypoxic encephalopathy has resulted. …
Pour qui

Midazolam Injection is indicated: intramuscularly or intravenously for preoperative sedation/anxiolysis/amnesia; intravenously as an agent for sedation/anxiolysis/amnesia prior to or during diagnostic, therapeutic or endoscopic procedures, such as bronchoscopy, gastroscopy, cystoscopy, coronary angiography, cardiac catheterization, oncology procedures, radiologic procedures, suture of lacerations and other procedures either alone or in combination with other CNS depressants; intravenously for induction of general anesthesia, before administration of other anesthetic agents. …

Comment le prendre et à quelle fréquence
  • NOTE: CONTAINS BENZYL ALCOHOL (see WARNINGS and PRECAUTIONS: PEDIATRIC USE) The 1 mL and 2 mL Midazolam Injection vials include a cautionary label that extends above the main label and highlights the drug name and strength per total volume
  • The purpose of the extended label is to prevent medication errors due to the different strengths of Midazolam Injection
  • Read the label and confirm you have selected the correct medication and strength
  • Then locate the "Tear Here" point on the label, and remove this cautionary label prior to removing the flip-off cap
  • Midazolam is a potent sedative agent that requires slow administration and individualization of dosage
  • Clinical experience has shown midazolam to be 3 to 4 times as potent per mg as diazepam
  • BECAUSE SERIOUS AND LIFE-THREATENING CARDIORESPIRATORY ADVERSE EVENTS HAVE BEEN REPORTED, PROVISION FOR MONITORING, DETECTION AND CORRECTION OF THESE REACTIONS MUST BE MADE FOR EVERY PATIENT TO WHOM MIDAZOLAM INJECTION IS ADMINISTERED, REGARDLESS OF AGE OR HEALTH STATUS
  • Excessive single doses or rapid intravenous administration may result in respiratory depression, airway obstruction and/or arrest
  • The potential for these latter effects is increased in debilitated patients, those receiving concomitant medications capable of depressing the CNS, and patients without an endotracheal tube but undergoing a procedure involving the upper airway such as endoscopy or dental (see BOXED WARNING and WARNINGS.) Reactions such as agitation, involuntary movements, hyperactivity and combativeness have been reported in adult and pediatric patients. …
Talk to a doctor first if
  • Injectable midazolam is contraindicated in patients with a known hypersensitivity to the drug
  • Benzodiazepines are contraindicated in patients with acute narrow-angle glaucoma
  • Benzodiazepines may be used in patients with open-angle glaucoma only if they are receiving appropriate therapy
  • Measurements of intraocular pressure in patients without eye disease show a moderate lowering following induction with midazolam; patients with glaucoma have not been studied. …
Warnings

Personnel and Equipment for Monitoring and Resuscitation Prior to the intravenouse administration of midazolam in any dose, the immediate availability of oxygen, resuscitative drugs, age- and size-appropriate equipment for bag/valve/mask ventilation and intubation, and skilled personnel for the maintenance of a patent airway and support of ventilation should be ensured. patients should be continuously monitored for early signs of hypoventilation, airway obstruction, or apnea with means readily available (e.g., pulse oximetry). hypoventilation, airway obstruction, and apnea can lead to hypoxia and/or cardiac arrest unless effective countermeasures are taken immediately. …

Effets secondaires possibles

See WARNINGS concerning serious cardiorespiratory events and possible paradoxical reactions. Fluctuations in vital signs were the most frequently seen findings following parenteral administration of midazolam in adults and included decreased tidal volume and/or respiratory rate decrease (23.3% of patients following IV and 10.8% of patients following IM administration) and apnea (15.4% of patients following IV administration), as well as variations in blood pressure and pulse rate. …

If you take too much

Symptoms The manifestations of midazolam overdosage reported are similar to those observed with other benzodiazepines, including sedation, somnolence, confusion, impaired coordination, diminished reflexes, coma and untoward effects on vital signs. No evidence of speficic organ toxicity from midazolam overdosage has been reported. Treatment Treatment of injectable midazolam overdosage is the same as that followed for overdosage with other benzodiazepines. Respiration, pulse rate and blood pressure should be monitored and general supportive measures should be employed. …

Dépendance et mésusage

Midazolam injection contains midazolam, a Schedule IV controlled substance. Midazolam was actively self-administered in primate models used to assess the positive reinforcing effects of psychoactive drugs. Midazolam produced physical dependence of a mild to moderate intensity in cynomolgus monkeys after 5 to 10 weeks of administration. Available data concerning the drug abuse and dependence potential of midazolam suggest that its abuse potential is at least equivalent to that of diazepam. …

How to store it

STORAGE Store at 20°-25°C (68°-77°F), excursions permitted to 15°-30°C (59°-86°F) [See USP Controlled Room Temperature].

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

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 2025-10-31.

Label for midazolam (midazolam hydrochloride), the active ingredient registered with NAFDAC.

Check your pack of Midashin 5 mg/mL Injection

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

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Encore 3 vérifications gratuites aujourd'hui Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Midashin 5 mg/mL Injection

What is in Midashin 5 mg/mL Injection?

Midashin 5 mg/mL Injection contains Midazolam (Midazolam Hydrochloride) (5 mg/mL), as injection, according to its NAFDAC registration record.

Is Midashin 5 mg/mL Injection registered with NAFDAC?

Yes. Midashin 5 mg/mL Injection is listed on the NAFDAC register under registration number A4-101180, and its registration is active as of 4 November 2026.

Has Midashin 5 mg/mL Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Midashin 5 mg/mL Injection in our automatically synced alert list.

How can I check that my pack of Midashin 5 mg/mL Injection is genuine?

Run a free authenticity scan with the NAFDAC number A4-101180, 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.

Do I need a prescription for Midashin 5 mg/mL Injection?

Yes. Midashin 5 mg/mL Injection contains midazolam, a controlled medicine. Prescription only. A licensed pharmacist may sell it only against a doctor's prescription.

How do I take Midashin 5 mg/mL Injection?

Follow your prescription or the leaflet in your pack. The official label says: NOTE: CONTAINS BENZYL ALCOHOL (see WARNINGS and PRECAUTIONS: PEDIATRIC USE) The 1 mL and 2 mL Midazolam Injection vials include a cautionary label that extends above the main label and highlights the drug name and strength per total volume. The purpose of the extended label is to prevent medication errors due to the different strengths of Midazolam Injection. Read the label and…

What is Midashin 5 mg/mL Injection used for?

Midazolam Injection is indicated: intramuscularly or intravenously for preoperative sedation/anxiolysis/amnesia; intravenously as an agent for sedation/anxiolysis/amnesia prior to or during diagnostic, therapeutic or endoscopic procedures, such as bronchoscopy, gastroscopy, cystoscopy, coronary angiography, cardiac catheterization, oncology procedures, radiologic procedures, suture of lacerations (Summarised from the official U.S. FDA label for midazolam (midazolam hydrochloride). Always follow your doctor or pharmacist.)

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