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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127638691 | 12763869 | 1 | I | 2016 | 20160914 | 20160920 | 20160920 | EXP | US-PFIZER INC-2016433921 | PFIZER | 0.00 | A | F | Y | 0.00000 | 20160920 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127638691 | 12763869 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 100 MG, 1X/DAY | J95648 | 21992 | 100 | MG | PROLONGED-RELEASE TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127638691 | 12763869 | 1 | Depression |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127638691 | 12763869 | HO |
127638691 | 12763869 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127638691 | 12763869 | Abnormal behaviour | |
127638691 | 12763869 | Ankle fracture | |
127638691 | 12763869 | Blood pressure decreased | |
127638691 | 12763869 | Bradyphrenia | |
127638691 | 12763869 | Depressed mood | |
127638691 | 12763869 | Disorientation | |
127638691 | 12763869 | Fall | |
127638691 | 12763869 | Hypoacusis | |
127638691 | 12763869 | Irritability | |
127638691 | 12763869 | Loss of consciousness | |
127638691 | 12763869 | Sensory loss |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |