Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Buprenorphine hydrochloride
Drug ID BADD_D00311
Description Buprenorphine is a weak partial mu-opioid receptor agonist and a weak kappa-opioid receptor antagonist used for the treatment of severe pain.[A186283,A186292] It is also commonly used as an alternative to [methadone] for the treatment of severe opioid addiction.[F4715,F4718] Buprenorphine is commercially available as the brand name product Suboxone which is formulated in a 4:1 fixed-dose combination product along with [naloxone], a non-selective competitive opioid receptor antagonist. Combination with naloxone is intended to reduce the abuse potential of Suboxone, as naloxone is poorly absorbed by the oral route (and has no effect when taken orally), but would reverse the opioid agonist effects of buprenorphine if injected intravenously.[A186289,F4715,F4718] Buprenorphine has poor gastrointestinal absorption and is therefore formulated as a sublingual tablet.
Indications and Usage For the treatment of moderate to severe pain, peri-operative analgesia, and opioid dependence.
Marketing Status Prescription; Discontinued
ATC Code N02AE01; N07BC01
DrugBank ID DB00921
KEGG ID D00836
MeSH ID D002047
PubChem ID 3033050
TTD Drug ID D06AWE
NDC Product Code 50090-1571; 59385-022; 55700-867; 59385-025; 0409-2012; 59385-021; 63275-9922; 42023-179; 0517-0725; 12496-0757; 0792-0634; 62991-1583; 38779-0888; 12578-608; 47848-007; 59385-024; 59385-027; 50383-924; 0406-2910; 50383-930; 0792-0630; 59385-023; 10920-590; 51927-0140; 62756-316; 73548-0608; 71795-1100; 49452-8253; 0406-2933; 67509-008; 0143-9246; 59385-026; 65267-104; 51927-1012; 12707-035; 53747-012; 61960-9064; 0406-3210; 57587-924; 57587-930; 51634-0608; 63629-7125
Synonyms Buprenorphine | Buprenex | Prefin | Subutex | Buprex | Temgesic | Temgésic | 6029-M | 6029 M | 6029M | RX-6029-M | RX 6029 M | RX6029M | Buprenorphine Hydrochloride | Hydrochloride, Buprenorphine
Chemical Information
Molecular Formula C29H42ClNO4
CAS Registry Number 53152-21-9
SMILES CC(C)(C)C(C)(C1CC23CCC1(C4C25CCN(C3CC6=C5C(=C(C=C6)O)O4)CC7CC7)OC)O.Cl
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal pain07.01.05.002--
Abscess11.01.08.001--Not Available
Adrenal insufficiency05.01.02.001; 14.11.01.004--
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Androgen deficiency21.16.02.001; 05.05.02.008--
Anxiety19.06.02.002--
Asthenia08.01.01.001--Not Available
Back pain15.03.04.005--
Chills15.05.03.016; 08.01.09.001--
Constipation07.02.02.001--
Cough22.02.03.001--
Depression19.15.01.001--
Diarrhoea07.02.01.001--
Dizziness17.02.05.003; 02.01.02.004; 24.06.02.007--
Dyspepsia07.01.02.001--
Headache17.14.01.001--
Hyperhidrosis23.02.03.004; 08.01.03.028--
Infection11.01.08.002--Not Available
Influenza22.07.02.001; 11.05.03.001--Not Available
Injury12.01.08.004--Not Available
Insomnia19.02.01.002; 17.15.03.002--
Lacrimation increased06.08.02.004--
Nausea07.01.07.001--
Nervousness19.06.02.003--Not Available
Pain08.01.08.004--
Pharyngitis22.07.03.004; 11.01.13.003; 07.05.07.004--
Pyrexia08.05.02.003--
Rhinitis11.01.13.004; 22.07.03.006--
Serotonin syndrome17.05.02.004; 15.05.04.016; 12.03.01.041--Not Available
Somnolence19.02.05.003; 17.02.04.006--
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