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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125632041 | 12563204 | 1 | I | 20160709 | 20160715 | 20160715 | PER | US-PFIZER INC-2016338649 | PFIZER | 0.00 | M | Y | 0.00000 | 20160715 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125632041 | 12563204 | 1 | PS | GABAPENTIN. | GABAPENTIN | 1 | 100 MG, 3X/DAY | U | 20235 | 100 | MG | CAPSULE, HARD | TID | ||||||
125632041 | 12563204 | 2 | SS | OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | [OXYCODONE HYDROCHLORIDE, 10MG]/[PARACETAMOL, 325 MG] | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125632041 | 12563204 | 1 | Neuralgia |
125632041 | 12563204 | 2 | Pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125632041 | 12563204 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125632041 | 12563204 | Back pain | |
125632041 | 12563204 | Feeling abnormal | |
125632041 | 12563204 | Insomnia | |
125632041 | 12563204 | Malaise | |
125632041 | 12563204 | Muscle twitching | |
125632041 | 12563204 | Myalgia | |
125632041 | 12563204 | Nerve injury | |
125632041 | 12563204 | Product use issue | |
125632041 | 12563204 | Restlessness | |
125632041 | 12563204 | Tremor |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |