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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125594911 | 12559491 | 1 | I | 20160630 | 20160715 | 20160715 | PER | US-PFIZER INC-2016328784 | PFIZER | 49.00 | YR | M | Y | 0.00000 | 20160715 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125594911 | 12559491 | 1 | PS | EFFEXOR XR | VENLAFAXINE HYDROCHLORIDE | 1 | 75 MG, UNK | U | 20699 | 75 | MG | PROLONGED-RELEASE CAPSULE |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125594911 | 12559491 | Chills | |
125594911 | 12559491 | Decreased appetite | |
125594911 | 12559491 | Diplopia | |
125594911 | 12559491 | Disturbance in attention | |
125594911 | 12559491 | Feeling of body temperature change | |
125594911 | 12559491 | Impaired driving ability | |
125594911 | 12559491 | Insomnia | |
125594911 | 12559491 | Muscle spasms | |
125594911 | 12559491 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |