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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126197702 | 12619770 | 2 | F | 20160304 | 20160803 | 20160803 | 20160808 | EXP | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-50071BP | BOEHRINGER INGELHEIM | 81.00 | YR | M | Y | 0.00000 | 20160808 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126197702 | 12619770 | 1 | PS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | Oral | 300 MG | U | 22512 | 150 | MG | CAPSULE | BID | |||||
| 126197702 | 12619770 | 2 | SS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | U | 22512 | |||||||||||
| 126197702 | 12619770 | 3 | C | NORVASC | AMLODIPINE BESYLATE | 1 | Oral | 5 MG | 0 | 5 | MG | CAPSULE | QD | ||||||
| 126197702 | 12619770 | 4 | C | ZOCOR | SIMVASTATIN | 1 | Oral | 0 | TABLET | ||||||||||
| 126197702 | 12619770 | 5 | C | LYRICA | PREGABALIN | 1 | Oral | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126197702 | 12619770 | 1 | Cerebrovascular accident prophylaxis |
| 126197702 | 12619770 | 2 | Atrial fibrillation |
| 126197702 | 12619770 | 3 | Hypertension |
| 126197702 | 12619770 | 4 | Blood cholesterol increased |
| 126197702 | 12619770 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126197702 | 12619770 | HO |
| 126197702 | 12619770 | OT |
| 126197702 | 12619770 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126197702 | 12619770 | Cerebral haemorrhage | |
| 126197702 | 12619770 | Death |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |