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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126813332 | 12681333 | 2 | F | 20160823 | 20160824 | 20160829 | EXP | US-PFIZER INC-2016400011 | PFIZER | 52.00 | YR | F | Y | 0.00000 | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126813332 | 12681333 | 1 | PS | GABAPENTIN. | GABAPENTIN | 1 | 300 MG, 3X/DAY | U | 20235 | 300 | MG | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126813332 | 12681333 | 1 | Neuropathy peripheral |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126813332 | 12681333 | HO |
| 126813332 | 12681333 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126813332 | 12681333 | Balance disorder | |
| 126813332 | 12681333 | Central nervous system lesion | |
| 126813332 | 12681333 | Dizziness | |
| 126813332 | 12681333 | Fall | |
| 126813332 | 12681333 | Gait disturbance | |
| 126813332 | 12681333 | Inner ear disorder | |
| 126813332 | 12681333 | 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 |