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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126993721 | 12699372 | 1 | I | 20160825 | 20160830 | 20160830 | EXP | AU-PFIZER INC-2016402957 | PFIZER | 0.00 | F | Y | 0.00000 | 20160830 | CN | AU | AU |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126993721 | 12699372 | 1 | PS | NEURONTIN | GABAPENTIN | 1 | UNK | U | 20235 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126993721 | 12699372 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126993721 | 12699372 | Dizziness | |
126993721 | 12699372 | Fall | |
126993721 | 12699372 | Infection | |
126993721 | 12699372 | Lower limb fracture |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |