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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126344172 | 12634417 | 2 | F | 20160809 | 20160808 | 20160823 | PER | US-BAYER-2016-151713 | BAYER | 0.00 | E | F | Y | 0.00000 | 20160823 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126344172 | 12634417 | 1 | PS | CLIMARA PRO | ESTRADIOLLEVONORGESTREL | 1 | Transdermal | UNK | 150148 | 21258 | TRANSDERMAL PATCH | ||||||||
| 126344172 | 12634417 | 2 | SS | CLIMARA PRO | ESTRADIOLLEVONORGESTREL | 1 | Transdermal | UNK | 21258 | TRANSDERMAL PATCH |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126344172 | 12634417 | 1 | Skin disorder |
| 126344172 | 12634417 | 2 | Skin disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126344172 | 12634417 | Expired device used | |
| 126344172 | 12634417 | Intentional product use issue | |
| 126344172 | 12634417 | Product packaging issue | |
| 126344172 | 12634417 | Product physical issue | |
| 126344172 | 12634417 | Product quality issue | |
| 126344172 | 12634417 | Product use issue | |
| 126344172 | 12634417 | Therapeutic response unexpected |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |