Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Urofollitropin
Drug ID BADD_D02319
Description Urofollitropin is a urinary-derived follicle-stimulating hormone (FSH) that is extracted and purified from human urine samples. It consists of two non-covalently linked, non-identical glycoproteins designated as the alpha- and beta- subunits. The alpha- and beta- subunits have 92 and 111 amino acids. The alpha subunit is glycosylated at Asn 51 and Asn 78 while the beta subunit is glycosylated at Asn 7 and Asn 24. Urofollitropin is typically used injected subcutaneously in combination with human chorionic gonadotropin (hCG) to induce ovulation. Urofollitropin may also be used to cause the ovary to produce several follicles, which can then be harvested for use in gamete intrafallopian transfer (GIFT) or in vitro fertilization (IVF).
Indications and Usage For treatment of female infertility
Marketing Status approved; vet_approved
ATC Code G03GA04
DrugBank ID DB00094
KEGG ID D06269
MeSH ID D050477
PubChem ID 62819
TTD Drug ID D02SBQ
NDC Product Code 76403-5002; 71052-066; 76403-5001
UNII W9BB98U6HP
Synonyms Urofollitropin | Follicle-Stimulating Hormone, Human Urine | Follicle Stimulating Hormone, Human Urine | Human FSH, Urinary | Urinary Human FSH | Fertinex | Metrodin | Neo Fertinorm | Metrodin HP | Metrodin High Purity | High Purity, Metrodin | Bravelle | Follitrin
Chemical Information
Molecular Formula C42H65N11O12S2
CAS Registry Number 26995-91-5
SMILES CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(CSSCC(C(=O)NC(C(=O)N1)CC2=CC=C(C=C2)O)N)C(=O)N3C CCC3C(=O)NC(CC(C)C)C(=O)NCC(=O)N)CC(=O)N)C(C)O
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)
Abdominal discomfort07.01.06.001--Not Available
Abdominal distension07.01.04.001--
Abdominal pain07.01.05.002--
Abdominal pain lower07.01.05.010--Not Available
Abdominal pain upper07.01.05.003--
Abnormal faeces07.01.03.001--Not Available
Abortion spontaneous18.01.04.001--Not Available
Abscess11.01.08.001--Not Available
Acne23.02.01.001--Not Available
Acute respiratory distress syndrome24.03.02.034; 10.02.01.067; 22.01.03.001--
Aggression19.05.01.001--Not Available
Agitation19.06.02.001; 17.02.05.012--
Alanine aminotransferase increased13.03.04.005--
Alopecia23.02.02.001--
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.003--Not Available
Angioedema23.04.01.001; 10.01.05.009; 22.04.02.008--Not Available
Anovulatory cycle21.01.01.011; 05.05.01.017--Not Available
Anxiety19.06.02.002--
Aplastic anaemia01.03.03.002--Not Available
Application site oedema12.07.01.020; 08.02.01.020--Not Available
Arthralgia15.01.02.001--
Arthropathy15.01.01.003--Not Available
Aspartate aminotransferase increased13.03.04.011--
Assisted fertilisation25.10.04.001--Not Available
Asthenia08.01.01.001--Not Available
Asthma22.03.01.002; 10.01.03.010--Not Available
Ataxia17.02.02.001; 08.01.02.004--
Atelectasis22.01.02.001--
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