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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125864713 | 12586471 | 3 | F | 20160831 | 20160725 | 20160913 | PER | US-PFIZER INC-2016211430 | PFIZER | 0.00 | F | Y | 0.00000 | 20160913 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125864713 | 12586471 | 1 | SS | ELIQUIS | APIXABAN | 1 | Unknown | UNK | U | 0 | FILM-COATED TABLET | ||||||||
| 125864713 | 12586471 | 2 | PS | LYRICA | PREGABALIN | 1 | Unknown | UNK | U | 21446 | |||||||||
| 125864713 | 12586471 | 3 | SS | HYDROCODONE | HYDROCODONE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125864713 | 12586471 | 1 | Cardiac disorder |
| 125864713 | 12586471 | 2 | Back pain |
| 125864713 | 12586471 | 3 | Pain |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125864713 | 12586471 | Pain in extremity | |
| 125864713 | 12586471 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |