Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Finasteride
Drug ID BADD_D00898
Description Finasteride is a synthetic 4-azasteroid compound [L10565] and specific inhibitor of steroid Type II 5α-reductase, which is an intracellular enzyme that converts the androgen testosterone into 5α-dihydrotestosterone (DHT). It works in a similar fashion as [dutasteride], which is another 5-alpha-reductase inhibitor, by exerting antiandrogenic effects. Finasteride is an orally active drug that was first approved by the FDA in 1992 for the treatment of benign prostatic hyperplasia to improve symptoms and reduce the risk for acute urinary retention or the need for surgical procedures.[L6244,L10565] In 1998, it was approved by the FDA to treat male pattern hair loss.[L6244] Finasteride is commonly marketed under the brand names Propecia and Proscar to be used aloneo or in combination with [doxazosin], an alpha-blocker. Both benign prostatic hyperplasia and androgenic alopecia are androgen-dependent disorders that are characterized by _in situ_ high levels of DHT.[A178159] In the treatment of benign prostate hyperplasia, alpha-blockers such as [tamsulosin] and [terazosin] are also used. Compared to alpha-blockers that focus on providing the rapid relief of symptoms, 5α-reductase inhibitors aim to target the underlying disease by blocking the effects of the primary androgen involved in benign prostate hyperplasia and androgenic alopecia, thus reducing the risk for secondary complications while providing symptom control.[A2132]
Indications and Usage Finasteride is indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate to improve symptoms, reduce the risk of acute urinary retention, and reduce the risk of the need for surgery including transurethral resection of the prostate (TURP) and prostatectomy.[L10565] A combination product with [tadalafil] is also used for the symptomatic treatment of BPH for up to 26 weeks.[L39439] Finasteride is also indicated for the treatment of male pattern hair loss (androgenetic alopecia, hereditary alopecia, or common male baldness) in male patients.[L6235]
Marketing Status approved
ATC Code D11AX10; G04CB01
DrugBank ID DB01216
KEGG ID D00321
MeSH ID D018120
PubChem ID 57363
TTD Drug ID D08IWD
NDC Product Code 65862-370; 50090-4648; 68071-1648; 71205-790; 71335-1898; 71713-096; 38779-2410; 64918-0422; 31722-526; 55154-8083; 65862-927; 68788-8377; 70518-2287; 71610-515; 49452-3147; 16729-090; 31722-525; 55111-171; 61919-733; 69097-112; 60687-428; 63187-265; 65862-149; 68071-3234; 68788-6976; 71335-0433; 71713-099; 71052-602; 0093-7355; 47335-715; 50268-314; 70518-3600; 76420-151; 51508-001; 51927-4847; 53104-7549; 62991-3175; 68382-074; 68645-541; 70518-3182; 76282-412; 50090-4697; 67877-455; 70518-0397; 70518-3616; 70771-1152; 71205-767; 71335-1304; 71335-1634; 76420-074; 0904-6830; 48087-0092; 68981-021; 43598-303; 47335-714; 55111-172; 67877-288; 68071-2999; 71610-520; 14501-0013; 53104-7714; 16729-089; 35573-400; 57237-061; 68071-2695; 71335-1530; 78206-153; 46144-345; 64918-0706; 68554-0022; 50090-1936; 57237-062; 63187-863; 68071-2620; 68071-3306; 68071-3417; 68788-8275; 70518-2363; 70518-3612; 76420-154; 78206-152; 82009-061; 51552-1470; 55111-026; 43598-390; 50090-1718
UNII 57GNO57U7G
Synonyms Finasteride | Chibro-Proscar | Chibro Proscar | Propecia | Propeshia | MK-906 | MK 906 | MK906 | Proscar | Eucoprost
Chemical Information
Molecular Formula C23H36N2O2
CAS Registry Number 98319-26-7
SMILES CC12CCC3C(C1CCC2C(=O)NC(C)(C)C)CCC4C3(C=CC(=O)N4)C
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)
Lentigo23.05.01.0110.000045%Not Available
Lethargy17.02.04.003; 08.01.01.008; 19.04.04.0040.000724%
Libido decreased21.03.02.005; 19.08.03.0010.016992%
Libido increased19.08.03.002; 21.03.02.0070.000166%
Lip swelling23.04.01.007; 10.01.05.005; 07.05.04.005--Not Available
Lipoatrophy23.07.01.001; 14.08.04.0060.000135%
Lipoma15.09.01.001; 16.18.01.0010.000616%Not Available
Listless19.04.04.003; 08.01.01.0120.000180%Not Available
Liver disorder09.01.08.0010.000243%Not Available
Lordosis15.10.04.0050.000067%
Loss of consciousness17.02.04.004--Not Available
Loss of libido19.08.03.0030.011127%Not Available
Lung consolidation22.01.02.0100.000045%Not Available
Lung infiltration22.01.02.0040.000045%Not Available
Lymphadenopathy01.09.01.0020.000575%Not Available
Lymphoma16.20.01.001; 01.12.01.0010.000045%Not Available
Malabsorption14.02.01.004; 07.17.01.0010.000112%
Malaise08.01.01.0030.001479%
Male orgasmic disorder21.03.02.019; 19.08.01.0060.001119%Not Available
Mass08.03.05.0030.000144%Not Available
Melanocytic naevus16.26.01.007; 23.10.01.0070.001007%Not Available
Memory impairment19.20.01.003; 17.03.02.0030.001816%
Meningioma17.20.01.005; 16.30.01.0050.000045%Not Available
Mental impairment19.21.02.003; 17.03.03.0020.000634%Not Available
Microcytic anaemia01.03.02.0080.000099%Not Available
Micturition disorder20.02.02.0050.000198%Not Available
Micturition urgency20.02.02.0060.000818%
Middle insomnia19.02.01.003; 17.15.03.0030.000166%Not Available
Migraine24.03.05.003; 17.14.02.0010.000544%Not Available
Migraine with aura17.14.02.002; 24.03.05.0050.000166%Not Available
The 11th Page    First    Pre   11 12 13 14 15    Next   Last    Total 30 Pages