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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126906383 | 12690638 | 3 | F | 20160821 | 20160901 | 20160826 | 20160907 | EXP | US-PFIZER INC-2016405629 | PFIZER | 58.00 | YR | M | Y | 130.10000 | KG | 20160907 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126906383 | 12690638 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 50 MG, 3X/DAY | 21446 | 50 | MG | CAPSULE, HARD | TID | ||||||
126906383 | 12690638 | 2 | SS | KEPPRA | LEVETIRACETAM | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126906383 | 12690638 | 1 | Neuropathy peripheral |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126906383 | 12690638 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126906383 | 12690638 | Amnesia | |
126906383 | 12690638 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |