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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125356842 | 12535684 | 2 | F | 20160511 | 20160718 | 20160707 | 20160801 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-119778 | RANBAXY | 89.00 | YR | F | Y | 74.00000 | KG | 20160801 | CN | ES | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125356842 | 12535684 | 1 | PS | Atorvastatin | ATORVASTATIN | 1 | Oral | Y | U | 76477 | 40 | MG | |||||||
| 125356842 | 12535684 | 2 | C | ASPIRIN. | ASPIRIN | 1 | Unknown | U | U | 0 | |||||||||
| 125356842 | 12535684 | 3 | C | DILTIAZEM. | DILTIAZEM | 1 | Unknown | U | U | 0 | |||||||||
| 125356842 | 12535684 | 4 | C | LAXIDO | POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE | 1 | Unknown | U | U | 0 | |||||||||
| 125356842 | 12535684 | 5 | C | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | Unknown | U | U | 0 | |||||||||
| 125356842 | 12535684 | 6 | C | VANCOMYCIN | VANCOMYCIN | 1 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125356842 | 12535684 | 1 | Blood cholesterol increased |
| 125356842 | 12535684 | 2 | Product used for unknown indication |
| 125356842 | 12535684 | 3 | Product used for unknown indication |
| 125356842 | 12535684 | 4 | Product used for unknown indication |
| 125356842 | 12535684 | 5 | Product used for unknown indication |
| 125356842 | 12535684 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125356842 | 12535684 | HO |
| 125356842 | 12535684 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125356842 | 12535684 | Blood creatine phosphokinase increased | |
| 125356842 | 12535684 | Rhabdomyolysis |
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 |
|---|---|---|---|---|---|---|
| 125356842 | 12535684 | 1 | 20160512 | 0 |