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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125623211 | 12562321 | 1 | I | 20160705 | 20160715 | 20160715 | EXP | SE-TEVA-674601ISR | TEVA | 77.00 | YR | M | Y | 0.00000 | 20160715 | OT | SE | SE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125623211 | 12562321 | 1 | PS | Atorvastatin | ATORVASTATIN | 1 | U | 78773 | 40 | MG | TABLET | ||||||||
125623211 | 12562321 | 2 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | U | 0 | 10 | MG | TABLET |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125623211 | 12562321 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125623211 | 12562321 | Arthralgia | |
125623211 | 12562321 | Chills | |
125623211 | 12562321 | Disturbance in attention | |
125623211 | 12562321 | Malaise | |
125623211 | 12562321 | Memory impairment | |
125623211 | 12562321 | Myalgia | |
125623211 | 12562321 | Pyrexia | |
125623211 | 12562321 | Suicidal ideation | |
125623211 | 12562321 | Vasculitis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |