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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126568162 | 12656816 | 2 | F | 20160816 | 20160816 | 20160825 | EXP | SK-MYLANLABS-2016M1034114 | MYLAN | ADAMCOVA M, STURDIK I, KOLLER T, PAYER J. [DRESS SYNDROME]. [CZECH]. VNITR-LEK 2016;62(4):334-7. | 0.00 | Y | 0.00000 | 20160825 | OT | SK | SK |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126568162 | 12656816 | 1 | PS | ALLOPURINOL. | ALLOPURINOL | 1 | Unknown | 300 MG, QD | Y | U | 18659 | 300 | MG | QD | |||||
| 126568162 | 12656816 | 2 | SS | DICLOFENAC | DICLOFENAC | 1 | Unknown | UNK | Y | U | 0 | ||||||||
| 126568162 | 12656816 | 3 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126568162 | 12656816 | 1 | Blood uric acid increased |
| 126568162 | 12656816 | 2 | Spinal pain |
| 126568162 | 12656816 | 3 | Hypothyroidism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126568162 | 12656816 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126568162 | 12656816 | Drug reaction with eosinophilia and systemic symptoms | |
| 126568162 | 12656816 | Drug-induced liver injury |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |