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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124230192 | 12423019 | 2 | F | 20160621 | 20160601 | 20160706 | PER | US-PFIZER INC-2016280164 | PFIZER | 55.00 | YR | M | Y | 0.00000 | 20160706 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124230192 | 12423019 | 1 | PS | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | Oral | UNK | Y | 19839 | |||||||||
124230192 | 12423019 | 2 | SS | SOMA | CARISOPRODOL | 1 | UNK | U | 0 | ||||||||||
124230192 | 12423019 | 3 | SS | ZYBAN | BUPROPION HYDROCHLORIDE | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124230192 | 12423019 | 1 | Depression |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124230192 | 12423019 | Diarrhoea | |
124230192 | 12423019 | Dizziness | |
124230192 | 12423019 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |