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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126514711 | 12651471 | 1 | I | 20160518 | 20160803 | 20160815 | 20160815 | EXP | FR-BAYER-2016-150425 | BAYER | 0.00 | Y | 0.00000 | 20160815 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126514711 | 12651471 | 1 | PS | LEVITRA | VARDENAFIL HYDROCHLORIDE TRIHYDRATE | 1 | Transplacental | 4 DF, ONCE | 21400 | 4 | DF | FILM-COATED TABLET | 1X | ||||||
| 126514711 | 12651471 | 2 | SS | LEPTICUR | TROPATEPINE HYDROCHLORIDE | 1 | Transplacental | 150 MG, ONCE | 0 | 150 | MG | 1X | |||||||
| 126514711 | 12651471 | 3 | SS | ADVIL | IBUPROFEN | 1 | Transplacental | 10 DF, ONCE | 0 | 10 | DF | 1X |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126514711 | 12651471 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126514711 | 12651471 | Tachycardia foetal |
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 |
|---|---|---|---|---|---|---|
| 126514711 | 12651471 | 1 | 20160518 | 20160518 | 0 | |
| 126514711 | 12651471 | 2 | 20160518 | 20160518 | 0 | |
| 126514711 | 12651471 | 3 | 20160518 | 20160518 | 0 |