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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125618081 | 12561808 | 1 | I | 20160712 | 20160715 | 20160715 | EXP | US-PFIZER INC-2016343745 | PFIZER | 0.00 | F | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125618081 | 12561808 | 1 | PS | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | UNK | N | 19839 | ||||||||||
125618081 | 12561808 | 2 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | UNK | U | 21992 | PROLONGED-RELEASE TABLET | |||||||||
125618081 | 12561808 | 3 | SS | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | UNK | U | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125618081 | 12561808 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125618081 | 12561808 | Gastric infection | |
125618081 | 12561808 | Gastrointestinal disorder | |
125618081 | 12561808 | Malaise | |
125618081 | 12561808 | Nausea | |
125618081 | 12561808 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125618081 | 12561808 | 2 | 201602 | 0 |