Product image of Midazolam B. Braun (Midazolam Hydrochloride) supplied by GNH India

Midazolam B. Braun

Active Ingredient:
Midazolam Hydrochloride
Origin:
EU

Midazolam B. Braun (Midazolam Hydrochloride)

Midazolam, the active ingredient in Midazolam B. Braun, is a benzodiazepine presented as a sterile injectable solution for intramuscular, intravenous, or rectal use. It provides rapid sedation, anxiolysis, and anticonvulsant effects for patients undergoing procedures, anesthesia induction, or experiencing severe anxiety or seizures.
GNH India supplies Midazolam B. Braun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Midazolam is a benzodiazepine that acts on the central nervous system to produce sedation, anxiolysis, and seizure control.

  • Procedural sedation: provides rapid, controllable sedation and amnesia during minor surgeries or diagnostic procedures.
  • Induction of anesthesia: facilitates smooth transition to general anesthesia for surgical patients.
  • Status epilepticus: terminates ongoing seizures when first‑line therapies are insufficient.
  • Severe anxiety: reduces acute anxiety symptoms in pre‑operative or emergency settings.

How It Works

  • Midazolam binds to a specific site on the GABA‑A receptor complex, acting as a positive allosteric modulator. This enhances the inhibitory effect of the neurotransmitter GABA, increasing chloride ion influx and hyperpolarizing neuronal membranes, which leads to decreased neuronal excitability and produces sedation, anxiolysis, muscle relaxation, and anticonvulsant activity.

Side Effects

Midazolam may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Drowsiness: feeling unusually sleepy or lethargic.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Amnesia: short‑term memory loss for events occurring after administration.
  • Nausea: mild stomach upset or urge to vomit.
  • Hypotension: transient lowering of blood pressure.
  • Fatigue: general feeling of reduced energy.

Serious or Rare Side Effects

  • Severe respiratory depression: marked reduction in breathing effort that may require ventilation.
  • Apnea: temporary cessation of breathing.
  • Anaphylactic reaction: sudden, severe allergic response with rash, swelling, or airway compromise.
  • Paradoxical reactions: agitation, aggression, or involuntary movements.
  • Cardiac arrhythmia: irregular heart rhythm that may be life‑threatening.

Precautions & Warnings

Before using Midazolam, clinicians should consider several safety measures.

  • Assess respiratory function: monitor breathing and oxygen saturation continuously during and after dosing.
  • Evaluate hepatic impairment: adjust use in patients with significant liver disease.
  • Review concomitant CNS depressants: avoid additive sedation with opioids, alcohol, or other sedatives.
  • Consider age‑related sensitivity: elderly patients may require lower initial doses.
  • Monitor cardiovascular status: watch for hypotension or arrhythmias.
  • Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture and light.

Avoid Interactions

Midazolam can interact with other medicines, altering its effects or safety profile.

Major Interactions (Avoid)

  • Opioids (e.g., fentanyl, morphine): combined use can cause profound respiratory depression.
  • CNS depressants (e.g., barbiturates, alcohol): increase sedation and risk of overdose.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): raise plasma concentrations, leading to enhanced effects.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy by lowering drug levels.
  • Anticholinergic agents (e.g., atropine): can mask some sedative signs.
  • Antihypertensives (e.g., beta‑blockers): may augment blood‑pressure lowering effects.

Frequently Asked Questions

Midazolam B. Braun is a benzodiazepine indicated for procedural sedation, induction of general anesthesia, treatment of status epilepticus, and relief of severe acute anxiety. It is administered by injection to produce rapid onset of sedation and seizure control in hospital or clinical settings.

Midazolam enhances the activity of the neurotransmitter GABA at the GABA‑A receptor. By binding to a distinct site, it increases chloride ion flow into neurons, leading to hyperpolarization and reduced neuronal firing, which produces sedation, anxiolysis, muscle relaxation, and anticonvulsant effects.

The dose of Midazolam is individualized by the prescribing clinician based on the patient’s age, weight, clinical condition, route of administration, and response to therapy. No fixed regimen is provided here; dosing decisions are made at the point of care.

Safety data for Midazolam during pregnancy and lactation are limited. Because it crosses the placenta and may be excreted in breast milk, it is generally avoided unless the potential benefit justifies the potential risk to the fetus or infant.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and required import documentation.

Midazolam has a faster onset and shorter duration of action than diazepam, making it preferable for procedural sedation and anesthesia induction. Both are benzodiazepines, but Midazolam’s rapid pharmacokinetics allow tighter control of sedation depth, whereas diazepam is often used for longer‑acting anxiolysis.

Midazolam B. Braun should be stored at ambient temperature, below 25 °C, in its original sealed container. Protect the product from moisture, direct sunlight, and extreme temperature fluctuations. Do not freeze; discard any solution that appears discolored or contains particles.

Midazolam is supplied as a sterile injectable solution and can be given intravenously, intramuscularly, or rectally, depending on the clinical situation. The route, rate of injection, and monitoring requirements are determined by the treating physician and institutional protocols.

The most critical risks include severe respiratory depression, apnea, hypotension, and rare anaphylactic reactions. Continuous monitoring of breathing, oxygen saturation, and cardiovascular status is essential, especially when used with other central nervous system depressants.

Midazolam is contraindicated in patients with known hypersensitivity to benzodiazepines, severe respiratory insufficiency, acute narrow‑angle glaucoma, or those who are critically ill without adequate airway support. Caution is also advised for individuals with significant hepatic impairment or a history of paradoxical reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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