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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 108801532 | 10880153 | 2 | F | 20160912 | 20150302 | 20160916 | PER | US-PFIZER INC-2015070506 | PFIZER | 0.00 | M | Y | 0.00000 | 20160916 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 108801532 | 10880153 | 1 | PS | GABAPENTIN. | GABAPENTIN | 1 | 4000-5000 MGS PER DAY | U | 20235 | ||||||||||
| 108801532 | 10880153 | 2 | SS | GABAPENTIN. | GABAPENTIN | 1 | 4800 MG, 1X/DAY | U | 20235 | 4800 | MG | QD |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 108801532 | 10880153 | Drug ineffective | |
| 108801532 | 10880153 | Expired product administered | |
| 108801532 | 10880153 | Prescribed overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |