Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Medroxyprogesterone
Drug ID BADD_D01365
Description Medroxyprogesterone acetate (MPA) is a [progesterone] derivative that is more resistant to metabolism for improved pharmacokinetic properties.[A14848] MPA can be use to treat secondary amenorrhea, endometrial hyperplasia, abnormal uterine bleeding, osteoporosis, vasomotor symptoms in menopause, vulvar and vaginal atrophy, prevent pregnancy, manage pain in endometriosis, prevent pregnancy, and is also used in palliative care for endometrial and renal carcinoma.[L8657,L8660,L8663,L8666,L8669] Medroxyprogesterone acetate was granted FDA approval on 18 June 1959.[L8657]
Indications and Usage Used as a contraceptive and to treat secondary amenorrhea, abnormal uterine bleeding, pain associated with endometriosis, endometrial and renal cell carcinomas, paraphilia in males, GnRH-dependent forms of precocious puberty, as well as to prevent endometrial changes associated with estrogens.
Marketing Status Not Available
ATC Code G03AC06; G03DA02; L02AB02
DrugBank ID DB00603
KEGG ID D08166
MeSH ID D008525
PubChem ID 10631
TTD Drug ID D0I2SD
NDC Product Code 54348-805; 0009-0067
Synonyms Medroxyprogesterone | (6 alpha)-17-Hydroxy-6-methylpregn-4-ene-3,20-dione | Pregn-4-ene-3,20-dione, 17-hydroxy-6-methyl-, (6alpha)- | 17 alpha-Hydroxy-6 alpha-Methylprogesterone | 17 alpha Hydroxy 6 alpha Methylprogesterone | Methylhydroxyprogesterone | Adgyn Medro
Chemical Information
Molecular Formula C22H32O3
CAS Registry Number 520-85-4
SMILES CC1CC2C(CCC3(C2CCC3(C(=O)C)O)C)C4(C1=CC(=O)CC4)C
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Breast cancerMembrane progestin receptor alphaQ801D8Not Available7647339; 10622401; 10215033; 11196177; 9883987; 10424399; 2523869; 9563648
Breast cancerEstrogen receptorP03372T895347647339; 10622401; 10215033; 11196177; 9883987; 10424399; 2523869; 9563648
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal distension07.01.04.001--
Abdominal pain07.01.05.002--
Abscess11.01.08.001--Not Available
Acne23.02.01.001--Not Available
Alopecia23.02.02.001--
Amenorrhoea21.01.02.001; 05.05.01.002--
Anaemia01.03.02.001--
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--Not Available
Anorgasmia19.08.01.001--
Anovulatory cycle21.01.01.011; 05.05.01.017--Not Available
Anxiety19.06.02.002--
Arthralgia15.01.02.001--
Asthenia08.01.01.001--Not Available
Asthma22.03.01.002; 10.01.03.010--Not Available
Back pain15.03.04.005--
Bladder pain20.02.02.001--Not Available
Blindness17.17.01.003; 06.02.02.001--Not Available
Blood pressure increased13.14.03.005--Not Available
Body temperature increased13.15.01.001--Not Available
Bone disorder15.02.04.004--Not Available
Breast cancer16.10.01.001; 21.05.01.003--Not Available
Breast discharge21.05.05.001--Not Available
Breast mass21.05.04.002--Not Available
Breast pain21.05.05.003--
Breast tenderness21.05.05.004--Not Available
Bronchitis22.07.01.001; 11.01.09.001--
Cerebral thrombosis24.01.04.003; 17.08.01.006--Not Available
Cerebrovascular accident24.03.05.001; 17.08.01.007--
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