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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125916062 | 12591606 | 2 | F | 20160722 | 20160726 | 20160802 | EXP | SK-GLENMARK PHARMACEUTICALS S. R. O.-2016GMK023710 | GLENMARK | BAKOSOVA M, NEMSOVA J, BABAL P, STENOVA E.. SUBACUTE CUTANEOUS LUPUS ERYTHEMATOUS.. DERMA.. 2016;16 (2):3-6 | 71.00 | YR | F | Y | 0.00000 | 20160802 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125916062 | 12591606 | 1 | SS | Pantoprazole | PANTOPRAZOLE SODIUM | 1 | Unknown | 20 MG, QD | Y | 0 | 20 | MG | |||||||
| 125916062 | 12591606 | 2 | PS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | 20 MG, QD | Y | 91672 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125916062 | 12591606 | 1 | Dyspepsia |
| 125916062 | 12591606 | 2 | Dyspepsia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125916062 | 12591606 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125916062 | 12591606 | Dry mouth | |
| 125916062 | 12591606 | Fatigue | |
| 125916062 | 12591606 | Subacute cutaneous lupus erythematosus |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |