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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126346121 | 12634612 | 1 | I | 20160728 | 20160729 | 20160809 | 20160809 | PER | US-BAYER-2016-149875 | BAYER | 66.00 | YR | E | F | Y | 0.00000 | 20160809 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126346121 | 12634612 | 1 | PS | CLIMARA | ESTRADIOL | 1 | Transdermal | UNK MG, UNK | 150132 | 20375 | TRANSDERMAL PATCH | ||||||||
| 126346121 | 12634612 | 2 | C | ATENOLOL. | ATENOLOL | 1 | Oral | 50 MG, UNK | 0 | 50 | MG | ||||||||
| 126346121 | 12634612 | 3 | C | PRAVASTATIN. | PRAVASTATIN | 1 | Oral | 4 MG, UNK | 0 | ||||||||||
| 126346121 | 12634612 | 4 | C | TRAMTEREN COMP | 2 | Oral | 47.5 MG, UNK | 0 | |||||||||||
| 126346121 | 12634612 | 5 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Oral | 25 MG, UNK | 0 | ||||||||||
| 126346121 | 12634612 | 6 | C | RANITIDINE. | RANITIDINE | 1 | Oral | 150 MG, UNK | 0 | ||||||||||
| 126346121 | 12634612 | 7 | C | GABAPENTIN. | GABAPENTIN | 1 | Oral | 1500 MG, UNK | 0 | ||||||||||
| 126346121 | 12634612 | 8 | C | EZETIMIBE. | EZETIMIBE | 1 | Oral | 10 MG, UNK | 0 | ||||||||||
| 126346121 | 12634612 | 9 | C | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | Oral | 50 MG, UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126346121 | 12634612 | 1 | Menopausal symptoms |
| 126346121 | 12634612 | 9 | Insomnia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126346121 | 12634612 | Application site irritation | |
| 126346121 | 12634612 | Application site rash | |
| 126346121 | 12634612 | Discomfort | |
| 126346121 | 12634612 | Frustration tolerance decreased | |
| 126346121 | 12634612 | Product adhesion issue |
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 |
|---|---|---|---|---|---|---|
| 126346121 | 12634612 | 1 | 20160726 | 20160728 | 0 |