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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125670922 | 12567092 | 2 | F | 20160714 | 20160715 | 20160718 | 20160726 | PER | US-PFIZER INC-2016348652 | PFIZER | 60.00 | YR | F | Y | 74.84000 | KG | 20160726 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125670922 | 12567092 | 1 | PS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 75 MG, UNK | U | 20699 | 75 | MG | PROLONGED-RELEASE CAPSULE | ||||||
125670922 | 12567092 | 2 | SS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 150 MG, UNK | U | UNKNOWN | 20699 | 150 | MG | PROLONGED-RELEASE CAPSULE | |||||
125670922 | 12567092 | 3 | SS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 37.5 MG, 1X/DAY | U | 20699 | 37.5 | MG | PROLONGED-RELEASE CAPSULE | QD | |||||
125670922 | 12567092 | 4 | SS | LUVOX | FLUVOXAMINE MALEATE | 1 | 100 MG, UNK | U | 0 | 100 | MG | ||||||||
125670922 | 12567092 | 5 | C | LOSARTAN. | LOSARTAN | 1 | 100 MG, 1X/DAY | 0 | 100 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125670922 | 12567092 | 1 | Obsessive-compulsive disorder |
125670922 | 12567092 | 5 | Hypertension |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125670922 | 12567092 | Activities of daily living impaired | |
125670922 | 12567092 | Fatigue | |
125670922 | 12567092 | Nervousness | |
125670922 | 12567092 | Sluggishness | |
125670922 | 12567092 | Withdrawal syndrome |
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 |
---|---|---|---|---|---|---|
125670922 | 12567092 | 1 | 200401 | 0 |