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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126226141 | 12622614 | 1 | I | 2016 | 20160727 | 20160804 | 20160804 | EXP | FR-ASTRAZENECA-2016SE82418 | ASTRAZENECA | 77.00 | YR | M | Y | 84.00000 | KG | 20160804 | CN | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126226141 | 12622614 | 1 | PS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | 21366 | 5 | MG | TABLET | QD | |||||||
| 126226141 | 12622614 | 2 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | 21366 | 5 | MG | TABLET | QOD | |||||||
| 126226141 | 12622614 | 3 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | EVERY 3 DAYS | 21366 | TABLET | |||||||||
| 126226141 | 12622614 | 4 | C | METFORMINE | METFORMIN HYDROCHLORIDE | 1 | FOR AROUND 2 YEARS | 0 | |||||||||||
| 126226141 | 12622614 | 5 | C | TELMISARTAN. | TELMISARTAN | 1 | FOR AROUND 4 YEARS | 0 | |||||||||||
| 126226141 | 12622614 | 6 | C | INEXIUM | ESOMEPRAZOLE | 1 | PUNCTUALLY | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126226141 | 12622614 | 1 | Blood cholesterol abnormal |
| 126226141 | 12622614 | 2 | Blood cholesterol abnormal |
| 126226141 | 12622614 | 3 | Blood cholesterol abnormal |
| 126226141 | 12622614 | 4 | Glucose tolerance impaired |
| 126226141 | 12622614 | 5 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126226141 | 12622614 | HO |
| 126226141 | 12622614 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126226141 | 12622614 | Eye disorder | |
| 126226141 | 12622614 | Inguinal hernia | |
| 126226141 | 12622614 | Muscle atrophy | |
| 126226141 | 12622614 | Myalgia | |
| 126226141 | 12622614 | Off label use | |
| 126226141 | 12622614 | Pleural effusion | |
| 126226141 | 12622614 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |