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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126812831 | 12681283 | 1 | I | 20160817 | 20160824 | 20160824 | EXP | AU-MYLANLABS-2016M1035692 | MYLAN | BOYD I. THIAMAZOLE AND RHABDOMYOLYSIS. WHO-PHARM-NEWS 2016;4:17-23. | 0.00 | Y | 0.00000 | 20160824 | OT | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126812831 | 12681283 | 1 | PS | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | UNK | U | U | 90868 | ||||||||
| 126812831 | 12681283 | 2 | I | METHIMAZOLE. | METHIMAZOLE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 126812831 | 12681283 | 3 | C | ENALAPRIL | ENALAPRIL | 1 | Unknown | UNK | 0 | ||||||||||
| 126812831 | 12681283 | 4 | C | PHENPROCOUMON | PHENPROCOUMON | 1 | Unknown | UNK | 0 | ||||||||||
| 126812831 | 12681283 | 5 | C | PIRETANIDE | PIRETANIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 126812831 | 12681283 | 6 | C | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126812831 | 12681283 | 1 | Product used for unknown indication |
| 126812831 | 12681283 | 2 | Product used for unknown indication |
| 126812831 | 12681283 | 3 | Product used for unknown indication |
| 126812831 | 12681283 | 4 | Product used for unknown indication |
| 126812831 | 12681283 | 5 | Product used for unknown indication |
| 126812831 | 12681283 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126812831 | 12681283 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126812831 | 12681283 | Blood creatine phosphokinase increased | |
| 126812831 | 12681283 | Drug interaction | |
| 126812831 | 12681283 | Paresis | |
| 126812831 | 12681283 | Rhabdomyolysis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |