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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125877761 | 12587776 | 1 | I | 20160719 | 20160725 | 20160725 | EXP | US-PFIZER INC-2016352740 | PFIZER | 65.00 | YR | F | Y | 0.00000 | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125877761 | 12587776 | 1 | PS | VENLAFAXINE HCL | VENLAFAXINE HYDROCHLORIDE | 1 | 75 MG, 2X/DAY | Y | 20699 | 75 | MG | BID | |||||||
125877761 | 12587776 | 2 | C | ATENOLOL. | ATENOLOL | 1 | 50 MG, 1X/DAY | 0 | 50 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125877761 | 12587776 | 1 | Depression |
125877761 | 12587776 | 2 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125877761 | 12587776 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125877761 | 12587776 | Drug ineffective | |
125877761 | 12587776 | Drug intolerance | |
125877761 | 12587776 | Suicidal ideation |
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 |
---|---|---|---|---|---|---|
125877761 | 12587776 | 1 | 2009 | 2009 | 0 |