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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126655201 | 12665520 | 1 | I | 20150116 | 20160804 | 20160818 | 20160818 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-064578 | BRISTOL MYERS SQUIBB | 68.83 | YR | M | Y | 0.00000 | 20160818 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126655201 | 12665520 | 1 | PS | PRAVASTATIN SODIUM. | PRAVASTATIN SODIUM | 1 | Unknown | UNK | Y | 19898 | TABLET | ||||||||
| 126655201 | 12665520 | 2 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | Unknown | 20 MG, QD | Y | 0 | 20 | MG | QD | ||||||
| 126655201 | 12665520 | 3 | C | ATENOLOL. | ATENOLOL | 1 | Unknown | 1 DF, QD | U | 0 | 1 | DF | QD | ||||||
| 126655201 | 12665520 | 4 | C | IBUPROFEN. | IBUPROFEN | 1 | Unknown | UNK, QD | U | 0 | QD | ||||||||
| 126655201 | 12665520 | 5 | C | IBUPROFEN. | IBUPROFEN | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126655201 | 12665520 | 1 | Product used for unknown indication |
| 126655201 | 12665520 | 2 | Blood cholesterol |
| 126655201 | 12665520 | 3 | Blood pressure measurement |
| 126655201 | 12665520 | 4 | Back pain |
| 126655201 | 12665520 | 5 | Inflammation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126655201 | 12665520 | OT |
| 126655201 | 12665520 | HO |
| 126655201 | 12665520 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126655201 | 12665520 | Abasia | |
| 126655201 | 12665520 | Dizziness | |
| 126655201 | 12665520 | Fatigue | |
| 126655201 | 12665520 | Hypersensitivity | |
| 126655201 | 12665520 | Hypoaesthesia | |
| 126655201 | 12665520 | Myocardial infarction | |
| 126655201 | 12665520 | Restless legs syndrome |
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 |
|---|---|---|---|---|---|---|
| 126655201 | 12665520 | 1 | 20160125 | 20160218 | 0 | |
| 126655201 | 12665520 | 2 | 20151215 | 20160218 | 0 |