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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124413302 | 12441330 | 2 | F | 20160620 | 20160607 | 20160713 | PER | US-PFIZER INC-2016257629 | PFIZER | 59.00 | YR | F | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124413302 | 12441330 | 1 | PS | GABAPENTIN. | GABAPENTIN | 1 | 2700 MG, 1X/DAY | U | 20235 | 2700 | MG | QD | |||||||
| 124413302 | 12441330 | 2 | SS | GABAPENTIN. | GABAPENTIN | 1 | 1800 MG, 1X/DAY | U | 20235 | 1800 | MG | QD | |||||||
| 124413302 | 12441330 | 3 | C | LYRICA | PREGABALIN | 1 | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124413302 | 12441330 | Drug tolerance | |
| 124413302 | 12441330 | Intentional product use issue | |
| 124413302 | 12441330 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |