Overview
A barbiturate that is administered intravenously for the induction of general anesthesia or for the production of complete anesthesia of short duration. It is also used for hypnosis and for the control of convulsive states. It has been used in neurosurgical patients to reduce increased intracranial pressure. It does not produce any excitation but has poor analgesic and muscle relaxant properties. Small doses have been shown to be anti-analgesic and lower the pain threshold. (From Martindale, The Extra Pharmacopoeia, 30th ed, p920)
Indication
For use as the sole anesthetic agent for brief (15 minute) procedures, for induction of anesthesia prior to administration of other anesthetic agents, to supplement regional anesthesia, to provide hypnosis during balanced anesthesia with other agents for analgesia or muscle relaxation, for the control of convulsive states during or following inhalation anesthesia or local anesthesia, in neurosurgical patients with increased intracranial pressure, and for narcoanalysis and narcosynthesis in psychiatric disorders.
Associated Conditions
- Seizures
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/07/03 | Not Applicable | Completed | Melike Cengiz | ||
2017/04/07 | Phase 3 | Completed | |||
2015/07/01 | Not Applicable | Completed | |||
2015/03/04 | Phase 4 | Completed | |||
2011/12/20 | Phase 4 | Completed | |||
2009/08/25 | Phase 4 | Completed | |||
2008/10/07 | Not Applicable | Completed | |||
2008/02/25 | Phase 3 | Terminated | Hospital Universitari Son Dureta | ||
2008/02/11 | Not Applicable | Completed | |||
2007/07/20 | Phase 4 | Terminated |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
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No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
Pentothal thiopental sodium 500 mg powder for injection vial | 73505 | Link Medical Products Pty Ltd T/A Link Pharmaceuticals | Medicine | A | 3/21/2000 |
OMEGAPHARM THIOPENTAL SODIUM 470 mg thiopental sodium 470 mg powder for injection vial | 209478 | Medicine | A | 11/10/2015 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
PENTOTHAL READY TO MIX SYRINGE 250MG | hospira healthcare ulc | 00372536 | Powder For Solution - Intravenous | 250 MG / SYR | 12/31/1986 |
PENTOTHAL INJ 25MG/ML | hospira healthcare ulc | 00695017 | Powder For Solution - Intravenous | 25 MG / ML | 12/31/1988 |
PENTOTHAL SODIUM PWS 5GM | hospira healthcare ulc | 00038415 | Powder For Solution - Intravenous | 5 G / BOTTLE | 12/31/1975 |
PENTOTHAL SODIUM INJ 1GM STERILE | hospira healthcare ulc | 00038407 | Powder For Solution - Intravenous | 1 G / VIAL | 12/31/1951 |
PENTOTHAL INJ 500MG/SYR | hospira healthcare ulc | 00038393 | Powder For Solution - Intravenous | 500 MG | 12/31/1986 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
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No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
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