Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Alosetron hydrochloride
Drug ID BADD_D00083
Description Alosetron is a 5-HT3 antagonist used only for the management of severe diarrhoea-predominant irritable bowel syndrome (IBS) in women. Alosetron has an antagonist action on the 5-HT3 receptors and thus may modulate serotonin-sensitive gastrointestinal (GI) processes. Alosetron was voluntarily withdrawn from the US market in November 2000 by the manufacturer due to numerous reports of severe adverse effects including ischemic colitis, severely obstructed or ruptured bowel, and death. In June 2002, the FDA approved a supplemental new drug application allowing the remarketing of the drug under restricted conditions of use.
Indications and Usage Only for the treatment of symptoms of severe diarrhea-predominant irritable bowel syndrome (IBS) in women with chronic symptoms (generally lasting greater than 6 months) who does not present with anatomic or biochemical GI abnormalities and have not responded to conventional therapy.
Marketing Status approved; withdrawn
ATC Code A03AE01
DrugBank ID DB00969
KEGG ID D02829
MeSH ID C090840
PubChem ID 60758
TTD Drug ID D06GKN
NDC Product Code 76055-0009; 64980-453; 64980-454; 54766-894; 45963-480; 65162-248; 0054-0295; 0054-0296; 58159-032; 45963-479; 49884-819; 65162-249; 53104-7658; 49884-820; 54766-895
UNII 2F5R1A46YW
Synonyms alosetron | Lotronex | alosetron hydrochloride | alosetron monohydrochloride | 2,3,4,5-tetrahydro-5-methyl-2-((5-methylimidazol-4-yl)methyl)-1H-pyrido(4,3-b)indol-1-one monohydrochloride | GR 68755 | GR68755
Chemical Information
Molecular Formula C17H19ClN4O
CAS Registry Number 122852-69-1
SMILES CC1=C(N=CN1)CN2CCC3=C(C2=O)C4=CC=CC=C4N3C.Cl
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Muscle spasms15.05.03.004--
Myalgia15.05.02.001--
Nail disorder23.02.05.002--
Nausea07.01.07.001--
Pain08.01.08.004--
Pharyngitis22.07.03.004; 11.01.13.003; 07.05.07.004--
Photophobia06.01.01.004; 17.17.02.006--
Pollakiuria20.02.02.007--
Polyuria20.02.03.002--Not Available
Proctitis07.08.04.001--
Rash23.03.13.001--Not Available
Red blood cell count13.01.05.020--Not Available
Respiration abnormal22.02.01.041--Not Available
Rhinitis11.01.13.004; 22.07.03.006--
Sedation17.02.04.005--Not Available
Sexual dysfunction21.03.02.003; 19.08.05.002--Not Available
Skin infection23.11.04.007; 11.01.12.003--
Sweat gland disorder23.02.03.010--Not Available
Tenderness08.01.08.005--Not Available
Tooth impacted07.09.08.006--Not Available
Tremor17.01.06.002--
Ulcer08.03.06.001--Not Available
Urticaria23.04.02.001; 10.01.06.001--
Vaginal haemorrhage24.07.03.005; 21.08.01.001--
Vaginal infection21.14.02.002; 11.01.10.002--
Dermatosis23.03.03.017--Not Available
Tachyarrhythmia02.03.02.008--Not Available
Muscle tightness15.05.03.007--Not Available
Balance disorder17.02.02.007; 08.01.03.081--Not Available
Fluid imbalance14.05.01.003--Not Available
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