Estropipate
Ogen (estropipate) is a small molecule pharmaceutical. Estropipate was first approved as Ogen 5 on 1982-01-01. It is used to treat hot flashes, hypogonadism, menopause, menorrhagia, and premature menopause amongst others in the USA.
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Commercial
Trade Name
FDA
EMA
Ogen (discontinued: Estropipate, Ogen, Ortho-est)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
Brand Name | Status | Last Update |
|---|---|---|
| estropipate | ANDA | 2012-03-14 |
Agency Specific
FDA
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Clinical
Clinical Trials
34 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Infertility | D007246 | HP_0000789 | — | 1 | — | — | 1 | 1 | 3 |
| Contraception | D003267 | — | — | — | — | — | 1 | 1 | 2 |
| Physiological sexual dysfunction | D012735 | — | — | — | — | — | 1 | — | 1 |
Indications Phases 3
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Menopause | D008593 | EFO_0003922 | N95 | — | 2 | — | — | 4 | 6 |
| Breast neoplasms | D001943 | EFO_0003869 | C50 | 1 | 1 | — | — | 4 | 5 |
| Obesity | D009765 | EFO_0001073 | E66.9 | 1 | 2 | — | — | 1 | 4 |
| Syndrome | D013577 | — | — | — | 3 | — | — | 1 | 4 |
| Premenstrual syndrome | D011293 | — | N94.3 | — | 2 | — | — | — | 2 |
| Hot flashes | D019584 | — | — | — | 1 | — | — | 1 | 2 |
| Recurrence | D012008 | — | — | — | 1 | — | — | — | 1 |
| Hypersensitivity | D006967 | HP_0012393 | T78.40 | — | 1 | — | — | — | 1 |
| Habitual abortion | D000026 | EFO_1000954 | N96 | — | 1 | — | — | — | 1 |
| Atrophy | D001284 | — | — | — | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Female infertility | D007247 | EFO_0008560 | N97 | 1 | — | — | — | — | 1 |
| Healthy volunteers/patients | — | — | — | 1 | — | — | — | — | 1 |
| Therapeutic equivalency | D013810 | — | — | 1 | — | — | — | — | 1 |
| Aging | D000375 | GO_0007568 | R41.81 | 1 | — | — | — | — | 1 |
| Drug-related side effects and adverse reactions | D064420 | — | T88.7 | 1 | — | — | — | — | 1 |
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Kallmann syndrome | D017436 | Orphanet_478 | E23.0 | — | — | — | — | 1 | 1 |
| Primary ovarian insufficiency | D016649 | EFO_0004266 | E28.3 | — | — | — | — | 1 | 1 |
| Amenorrhea | D000568 | — | N91.2 | — | — | — | — | 1 | 1 |
| Ovarian hyperstimulation syndrome | D016471 | — | — | — | — | — | — | 1 | 1 |
| Premature menopause | D008594 | HP_0008209 | E28.31 | — | — | — | — | 1 | 1 |
| Venous thromboembolism | D054556 | EFO_0004286 | I74 | — | — | — | — | 1 | 1 |
| Thromboembolism | D013923 | HP_0001907 | — | — | — | — | — | 1 | 1 |
| Lacerations | D022125 | — | — | — | — | — | — | 1 | 1 |
| Female genital neoplasms | D005833 | — | — | — | — | — | — | 1 | 1 |
| Postmenopause | D017698 | — | — | — | — | — | — | 1 | 1 |
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Estropipate |
| INN | — |
| Description | Estropipate is a steroid sulfate and a piperazinium salt. It is functionally related to an estrone. |
| Classification | Small molecule |
| Drug class | estrogens; atropine derivatives |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | C1CNCCN1.C[C@]12CC[C@@H]3c4ccc(OS(=O)(=O)O)cc4CC[C@H]3[C@@H]1CCC2=O |
Identifiers
| PDB | — |
| CAS-ID | 7280-37-7 |
| RxCUI | — |
| ChEMBL ID | CHEMBL1200980 |
| ChEBI ID | — |
| PubChem CID | 5284555 |
| DrugBank | DB04574 |
| UNII ID | — |
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Estimated US medical usage
Estropipate
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Trends
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Additional graphs summarizing 103 documents
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Safety
Black-box Warning
Black-box warning for: Estropipate
Adverse Events
Top Adverse Reactions
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731 adverse events reported
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