Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Medroxyprogesterone acetate
Drug ID BADD_D01366
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 Medroxyprogesterone acetate (MPA) oral tablets are indicated to treat secondary amenorrhea, reduce the incidence of endometrial hyperplasia in postmenopausal women, and to treat abnormal uterine bleeding due to hormonal imbalance, not organic pathology.[L8657] Oral tablets containing MPA and conjugated estrogens are indicated to prevent postmenopausal osteoporosis and to treat moderate to severe menopausal symptoms such as vasomotor symptoms, vulvar atrophy, and vaginal atrophy.[L8660] Subcutaneous MPA is indicated to prevent pregnancy and manage pain associated with endometriosis.[L8663] Intramuscular MPA is indicated to prevent pregnancy,[L8666] and at higher concentrations for palliative treatment of endometrial or renal carcinoma.[L8669]
Marketing Status approved; investigational
ATC Code Not Available
DrugBank ID DB00603
KEGG ID D00951
MeSH ID D017258
PubChem ID 6279
TTD Drug ID Not Available
NDC Product Code 51552-0790; 60722-1006; 0009-0051; 0009-0746; 63629-8744; 63629-8825; 66993-370; 68788-8112; 0555-0872; 12866-1099; 16714-999; 0009-0065; 50090-5619; 50090-5747; 53002-3570; 63629-2612; 66993-371; 70518-3336; 38779-1422; 62991-1474; 50090-4251; 59762-0055; 55150-330; 55289-160; 59762-4537; 63629-8824; 67296-0396; 67457-887; 69097-539; 0548-5400; 46439-8749; 65089-0022; 16714-981; 0009-0287; 0009-7376; 62756-090; 70121-1480; 0548-5410; 65089-0002; 24201-150; 0009-4709; 50090-0490; 50090-0491; 68788-9899; 70518-3070; 0555-0873; 51927-0112; 59762-0056; 63187-382; 70121-1467; 0555-0779; 72789-043; 63592-0089; 55150-329; 59762-0058; 60687-105; 62756-091; 0548-5701; 52221-118; 0009-0286; 50090-0166; 50102-591; 0548-5711; 71205-118; 0009-5097; 46439-8712; 50090-3328; 63629-8826; 49452-4725; 50090-5925; 59762-4538
UNII C2QI4IOI2G
Synonyms Medroxyprogesterone Acetate | 6-alpha-Methyl-17alpha-hydroxyprogesterone Acetate | 6 alpha Methyl 17alpha hydroxyprogesterone Acetate | Depo-Medroxyprogesterone Acetate | Depo Medroxyprogesterone Acetate | (6 alpha)-17-(Acetoxy)-6-methylpregn-4-ene-3,20-dione | Pregn-4-ene-3,20-dione, 17-(acetyloxy)-6-methyl-, (6alpha)- | Medroxyprogesterone 17-Acetate | Medroxyprogesterone 17 Acetate | Depo-Provera | Depo Provera | DepoProvera | Farlutal | Gestapuran | Curretab | Medroxyprogesterone 17-Acetate, (6 beta)-Isomer | Perlutex | Provera | Veramix | Cycrin | Medroxyprogesterone 17-Acetate, (6 alpha,17 alpha)-Isomer
Chemical Information
Molecular Formula C24H34O4
CAS Registry Number 71-58-9
SMILES CC1CC2C(CCC3(C2CCC3(C(=O)C)OC(=O)C)C)C4(C1=CC(=O)CC4)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)
Vulvovaginal mycotic infection21.14.02.004; 11.03.05.004--Not Available
Bone loss15.02.04.0200.000119%Not Available
Sexually active26.05.02.001--Not Available
Low birth weight baby18.04.02.0030.000119%Not Available
Brain injury17.11.01.003; 19.07.03.0070.000119%Not Available
Vulvovaginal pain21.08.02.009--
Injury associated with device12.01.08.035; 08.07.01.0120.000559%Not Available
Microsomia08.01.03.056--Not Available
Mouth swelling23.04.01.020; 10.01.05.020; 07.05.04.0070.000119%Not Available
Complication associated with device08.07.01.0110.001047%Not Available
Alcohol interaction08.06.03.0030.000404%Not Available
Arrested labour18.07.03.0030.000119%Not Available
Malignant melanoma in situ16.03.01.004; 23.08.01.0040.000119%Not Available
Sleep disorder due to general medical condition, insomnia type19.02.04.004--Not Available
Self esteem decreased19.05.02.004--Not Available
Placenta accreta18.05.02.0030.000357%Not Available
Preterm premature rupture of membranes18.02.02.0160.000238%Not Available
Abnormal uterine bleeding21.01.01.013--Not Available
Anembryonic gestation18.01.03.007--Not Available
Attention deficit hyperactivity disorder19.21.04.004--Not Available
Bacterial vulvovaginitis21.14.02.013; 11.02.01.052--Not Available
Cerebral venous sinus thrombosis24.01.04.021; 17.08.03.0060.000238%Not Available
Congenital musculoskeletal disorder of skull15.11.02.011; 03.11.02.011--Not Available
Decidual cast21.07.01.023; 18.02.02.0190.000119%Not Available
Drug effective for unapproved indication12.09.02.001; 08.06.01.0370.000178%Not Available
Drug ineffective for unapproved indication12.09.02.002; 08.06.01.0380.002985%Not Available
Heavy menstrual bleeding21.01.03.0050.010621%Not Available
Idiopathic intracranial hypertension17.07.02.0110.000238%Not Available
Injection site indentation23.03.03.086; 12.07.03.061; 08.02.03.0610.000119%Not Available
Injection site scab12.07.03.069; 23.03.03.088; 08.02.03.0690.000262%Not Available
The 19th Page    First    Pre   19 20    Next   Last    Total 20 Pages