Product Details
Thiopental sodium for injection B.P
500MG/1GM
Product Description :
THIOPENTAL SODIUM FOR INJECTION B.P.
Sterile Powder for Solution for Intravenous Administration
COMPOSITION
Each vial contains:
Thiopental Sodium B.P. ............... 500 mg
or
Thiopental Sodium B.P. ............... 1 g
Excipients: As applicable.
PHARMACEUTICAL FORM
Sterile, yellowish to cream-coloured powder for solution for intravenous administration.
THERAPEUTIC CLASS
Ultra-short-acting Barbiturate
General Anaesthetic
INDICATIONS
Thiopental Sodium for Injection is indicated for use as an intravenous anaesthetic agent.
It may be used for:
• Induction of general anaesthesia
• Short surgical procedures
• Induction of anaesthesia prior to administration of other anaesthetic agents
• Control of certain convulsive states when clinically appropriate
• Reduction of intracranial pressure when controlled ventilation is provided, as clinically indicated
CONTRAINDICATIONS
Thiopental Sodium is contraindicated in patients with known hypersensitivity to thiopental or other barbiturates, or to any component of the formulation.
It is also contraindicated in patients with acute intermittent porphyria or a history of porphyria.
DRUG INTERACTIONS
Thiopental may interact with other medicines that produce central nervous system depression or affect anaesthesia.
Particular caution may be required with concomitant use of:
• Other general anaesthetic agents
• Opioid analgesics
• Sedative or hypnotic medicines
• Other central nervous system depressants
The anaesthetist should review all concomitant medications before administration.
ADMINISTRATION
Thiopental Sodium for Injection is intended for intravenous administration only.
The contents of the vial should be reconstituted with a suitable compatible diluent under appropriate aseptic conditions.
The reconstituted solution should be administered by a qualified healthcare professional experienced in intravenous anaesthesia.
For Intravenous Use Only.
STORAGE
Store according to the storage conditions stated on the approved product label.
Protect from excessive heat, moisture and light.
After reconstitution, use within the period specified in the approved product information.
Do not use if the reconstituted solution shows visible particles, precipitation or unexpected discoloration.