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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127306521 | 12730652 | 1 | I | 20160719 | 20160910 | 20160910 | PER | US-ASTRAZENECA-2016SE79344 | ASTRAZENECA | 0.00 | M | Y | 72.60000 | KG | 20160910 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127306521 | 12730652 | 1 | PS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | U | 21366 | 5 | MG | TABLET | QD | ||||||
| 127306521 | 12730652 | 2 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | TWO 5 MG TABLETS AT ONCE FOR A TOTAL DOSE OF 10MG EVERY OTHER DAY | U | 21366 | TABLET | ||||||||
| 127306521 | 12730652 | 3 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | TWO 5 MG TABLETS AT ONCE, TOTAL DOSE OF 10MG, FREQUENCY TWO TIMES PER WEEK | U | 21366 | TABLET | ||||||||
| 127306521 | 12730652 | 4 | SS | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | U | 0 | ||||||||||
| 127306521 | 12730652 | 5 | SS | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | U | 0 | ||||||||||
| 127306521 | 12730652 | 6 | C | INSULIN, HUMULOG, INJECTION | 2 | Unknown | 0 | ||||||||||||
| 127306521 | 12730652 | 7 | C | VITAMIN D3 WITH CALCIUM | 2 | Unknown | 0 | ||||||||||||
| 127306521 | 12730652 | 8 | C | IMODIUM | LOPERAMIDE HYDROCHLORIDE | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127306521 | 12730652 | 1 | Blood cholesterol increased |
| 127306521 | 12730652 | 2 | Blood cholesterol increased |
| 127306521 | 12730652 | 3 | Blood cholesterol increased |
| 127306521 | 12730652 | 6 | Diabetes mellitus |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127306521 | 12730652 | Abdominal pain upper | |
| 127306521 | 12730652 | Back pain | |
| 127306521 | 12730652 | Blood glucose increased | |
| 127306521 | 12730652 | Bowel movement irregularity | |
| 127306521 | 12730652 | Burning sensation | |
| 127306521 | 12730652 | Dehydration | |
| 127306521 | 12730652 | Diarrhoea | |
| 127306521 | 12730652 | Dizziness | |
| 127306521 | 12730652 | Drug dose omission | |
| 127306521 | 12730652 | Intentional product misuse | |
| 127306521 | 12730652 | Nonspecific reaction | |
| 127306521 | 12730652 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127306521 | 12730652 | 1 | 2013 | 0 | ||
| 127306521 | 12730652 | 2 | 2013 | 201510 | 0 | |
| 127306521 | 12730652 | 3 | 201601 | 0 | ||
| 127306521 | 12730652 | 4 | 201511 | 0 |