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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124908302 | 12490830 | 2 | F | 20160913 | 20160622 | 20160920 | EXP | NL-ASTRAZENECA-2016SE66440 | ASTRAZENECA | 0.00 | M | Y | 0.00000 | 20160921 | NL | NL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124908302 | 12490830 | 1 | PS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | 20.0MG UNKNOWN | U | 21366 | 20 | MG | TABLET | ||||||
124908302 | 12490830 | 2 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | 40.0MG UNKNOWN | U | 21366 | 40 | MG | TABLET |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124908302 | 12490830 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124908302 | 12490830 | Blood cholesterol increased | |
124908302 | 12490830 | Cerebrovascular accident | |
124908302 | 12490830 | Nightmare | |
124908302 | 12490830 | Product taste abnormal |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |