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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124436662 | 12443666 | 2 | F | 20160706 | 20160607 | 20160713 | EXP | US-PFIZER INC-2016260518 | PFIZER | 62.00 | YR | M | Y | 0.00000 | 20160713 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124436662 | 12443666 | 1 | PS | LYRICA | PREGABALIN | 1 | 50 MG | 21446 | 50 | MG | CAPSULE, HARD | ||||||||
| 124436662 | 12443666 | 2 | SS | GABAPENTIN. | GABAPENTIN | 1 | UNK | Y | 20235 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124436662 | 12443666 | 1 | Neuralgia |
| 124436662 | 12443666 | 2 | Neuralgia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124436662 | 12443666 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124436662 | 12443666 | Activities of daily living impaired | |
| 124436662 | 12443666 | Discomfort | |
| 124436662 | 12443666 | Drug ineffective | |
| 124436662 | 12443666 | Dysstasia | |
| 124436662 | 12443666 | Fatigue | |
| 124436662 | 12443666 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |