Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125665891 | 12566589 | 1 | I | 201604 | 20160504 | 20160718 | 20160718 | PER | US-MYLANLABS-2016M1019014 | MYLAN | 61.55 | YR | F | Y | 57.14000 | KG | 20160718 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125665891 | 12566589 | 1 | PS | ESTRADIOL TRANSDERMAL SYSTEM | ESTRADIOL | 1 | Transdermal | 0.1 MG/ QD, CHANGES TW | 615040 | 201675 | .1 | MG | TRANSDERMAL PATCH | QD | |||||
| 125665891 | 12566589 | 2 | SS | ESTRADIOL TRANSDERMAL SYSTEM | ESTRADIOL | 1 | Transdermal | 0.025 MG/ QD, CHANGES TW | 615024 | 201675 | .025 | MG | TRANSDERMAL PATCH | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125665891 | 12566589 | 1 | Menopausal symptoms |
| 125665891 | 12566589 | 2 | Menopausal symptoms |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125665891 | 12566589 | Drug effect decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125665891 | 12566589 | 1 | 2014 | 0 | ||
| 125665891 | 12566589 | 2 | 2014 | 0 |