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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126705031 | 12670503 | 1 | I | 20160809 | 20160822 | 20160822 | EXP | GR-CIPLA LTD.-2016GR17376 | CIPLA | 0.00 | Y | 0.00000 | 20160822 | OT | GB | GR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126705031 | 12670503 | 1 | PS | PRAVASTATIN. | PRAVASTATIN | 1 | Unknown | 20 MG, QD | U | U | 0 | 20 | MG | QD | |||||
| 126705031 | 12670503 | 2 | SS | PRAVASTATIN. | PRAVASTATIN | 1 | U | U | 0 | ||||||||||
| 126705031 | 12670503 | 3 | SS | PRAVASTATIN. | PRAVASTATIN | 1 | U | U | 0 | ||||||||||
| 126705031 | 12670503 | 4 | SS | ASPIRIN. | ASPIRIN | 1 | Oral | 80 MG, QD, LOW DOSE | U | U | 0 | 80 | MG | QD | |||||
| 126705031 | 12670503 | 5 | SS | ASPIRIN. | ASPIRIN | 1 | U | U | 0 | ||||||||||
| 126705031 | 12670503 | 6 | SS | ASPIRIN. | ASPIRIN | 1 | U | U | 0 | ||||||||||
| 126705031 | 12670503 | 7 | SS | METHYLDOPA. | METHYLDOPA | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126705031 | 12670503 | 1 | Antiphospholipid syndrome |
| 126705031 | 12670503 | 2 | Pre-eclampsia |
| 126705031 | 12670503 | 3 | Foetal growth restriction |
| 126705031 | 12670503 | 4 | Antiphospholipid syndrome |
| 126705031 | 12670503 | 5 | Pre-eclampsia |
| 126705031 | 12670503 | 6 | Foetal growth restriction |
| 126705031 | 12670503 | 7 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126705031 | 12670503 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126705031 | 12670503 | Exposure during pregnancy | |
| 126705031 | 12670503 | Premature delivery |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |