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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125267921 | 12526792 | 1 | I | 20160618 | 20160620 | 20160705 | 20160705 | PER | US-PFIZER INC-2016309872 | PFIZER | 55.00 | YR | M | Y | 81.65000 | KG | 20160705 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125267921 | 12526792 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 50 MG, DAILY | Y | 21992 | 50 | MG | PROLONGED-RELEASE TABLET | ||||||
125267921 | 12526792 | 2 | SS | GLUTEN | WHEAT GLUTEN | 1 | UNK | Y | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125267921 | 12526792 | 1 | Depression |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125267921 | 12526792 | Agitation | |
125267921 | 12526792 | Blood pressure increased | |
125267921 | 12526792 | Erythema | |
125267921 | 12526792 | Expired product administered | |
125267921 | 12526792 | Feeling hot | |
125267921 | 12526792 | Irritability | |
125267921 | 12526792 | Pruritus | |
125267921 | 12526792 | Urticaria |
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 |
---|---|---|---|---|---|---|
125267921 | 12526792 | 1 | 20160617 | 20160617 | 0 |