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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127410621 | 12741062 | 1 | I | 20160518 | 20160914 | 20160914 | PER | US-TEVA-662197USA | TEVA | 0.00 | M | Y | 78.09000 | KG | 20160914 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127410621 | 12741062 | 1 | PS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | 77056 | TABLET | ||||||||||
| 127410621 | 12741062 | 2 | SS | SOLMACK | HERBALS | 1 | Unknown | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127410621 | 12741062 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127410621 | 12741062 | Drug ineffective | |
| 127410621 | 12741062 | Hypoaesthesia oral | |
| 127410621 | 12741062 | Pruritus | |
| 127410621 | 12741062 | Rash | |
| 127410621 | 12741062 | Skin discolouration | |
| 127410621 | 12741062 | Throat tightness | |
| 127410621 | 12741062 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 127410621 | 12741062 | 1 | 2015 | 0 |