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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126000562 | 12600056 | 2 | F | 20160719 | 20160727 | 20160727 | PER | US-BAYER-2016-141417 | BAYER | 66.00 | YR | E | F | Y | 0.00000 | 20160727 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126000562 | 12600056 | 1 | PS | CLIMARA | ESTRADIOL | 1 | Transdermal | UNK | 20375 | TRANSDERMAL PATCH | |||||||||
126000562 | 12600056 | 2 | SS | CLIMARA | ESTRADIOL | 1 | Transdermal | UNK | 20375 | TRANSDERMAL PATCH |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126000562 | 12600056 | 1 | Hormone replacement therapy |
126000562 | 12600056 | 2 | Hormone replacement therapy |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126000562 | 12600056 | Application site erythema | |
126000562 | 12600056 | Intentional product misuse | |
126000562 | 12600056 | Menopausal symptoms | |
126000562 | 12600056 | Night sweats | |
126000562 | 12600056 | Product adhesion issue | |
126000562 | 12600056 | Skin irritation |
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 |
---|---|---|---|---|---|---|
126000562 | 12600056 | 1 | 201511 | 0 | ||
126000562 | 12600056 | 2 | 201603 | 0 |