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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125978712 | 12597871 | 2 | F | 20160624 | 20160822 | 20160727 | 20160829 | PER | US-PFIZER INC-2016358860 | PFIZER | 51.00 | YR | F | Y | 81.65000 | KG | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125978712 | 12597871 | 1 | PS | VENLAFAXINE HCL | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 75 MG, 1X/DAY | 375 | MG | Y | 20699 | 75 | MG | PROLONGED-RELEASE CAPSULE | QD | |||
125978712 | 12597871 | 2 | SS | VENLAFAXINE HCL | VENLAFAXINE HYDROCHLORIDE | 1 | 375 | MG | Y | 20699 | PROLONGED-RELEASE CAPSULE | ||||||||
125978712 | 12597871 | 3 | SS | VENLAFAXINE HCL | VENLAFAXINE HYDROCHLORIDE | 1 | 375 | MG | Y | 20699 | PROLONGED-RELEASE CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125978712 | 12597871 | 1 | Menopause |
125978712 | 12597871 | 2 | Depression |
125978712 | 12597871 | 3 | Panic attack |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125978712 | 12597871 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125978712 | 12597871 | Blood pressure increased | |
125978712 | 12597871 | Feeling abnormal | |
125978712 | 12597871 | Heart rate increased | |
125978712 | 12597871 | Hypersensitivity | |
125978712 | 12597871 | Lung disorder | |
125978712 | 12597871 | Musculoskeletal pain | |
125978712 | 12597871 | Myalgia | |
125978712 | 12597871 | Nervousness | |
125978712 | 12597871 | Pain | |
125978712 | 12597871 | Product colour issue |
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 |
---|---|---|---|---|---|---|
125978712 | 12597871 | 1 | 20160620 | 20160624 | 0 |