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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125510321 | 12551032 | 1 | I | 20160627 | 20160713 | 20160713 | EXP | SK-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-120027 | RANBAXY | 56.00 | YR | F | Y | 0.00000 | 20160713 | OT | GB | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125510321 | 12551032 | 1 | PS | ALLOPURINOL. | ALLOPURINOL | 1 | Unknown | 300 MG, DAILY | Y | 78390 | 300 | MG | |||||||
| 125510321 | 12551032 | 2 | SS | Diclofenac | DICLOFENAC | 1 | Unknown | Y | 0 | ||||||||||
| 125510321 | 12551032 | 3 | C | L-Thyroxine | LEVOTHYROXINE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125510321 | 12551032 | 1 | Blood uric acid increased |
| 125510321 | 12551032 | 2 | Spinal pain |
| 125510321 | 12551032 | 3 | Hypothyroidism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125510321 | 12551032 | HO |
| 125510321 | 12551032 | LT |
| 125510321 | 12551032 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125510321 | 12551032 | Drug reaction with eosinophilia and systemic symptoms | |
| 125510321 | 12551032 | 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 |