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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126413072 | 12641307 | 2 | F | 20160914 | 20160810 | 20160920 | PER | US-PFIZER INC-2016368964 | PFIZER | 67.00 | YR | F | Y | 63.28000 | KG | 20160920 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126413072 | 12641307 | 1 | PS | NEURONTIN | GABAPENTIN | 1 | Oral | 300MG IN EACH CAPSULE. TOOK TWO AT BEDTIME. ONCE A DAY | 20235 | 600 | MG | CAPSULE, HARD | |||||||
| 126413072 | 12641307 | 2 | SS | NEURONTIN | GABAPENTIN | 1 | Oral | 300 MG, 1X/DAY | 20235 | 300 | MG | CAPSULE, HARD | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126413072 | 12641307 | 1 | Neuralgia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126413072 | 12641307 | Peripheral swelling | |
| 126413072 | 12641307 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126413072 | 12641307 | 2 | 201607 | 0 |