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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
93436722 | 9343672 | 2 | F | 20160722 | 20130612 | 20160805 | EXP | FR-RANBAXY-2013US-70282 | RANBAXY | 88.00 | YR | F | Y | 0.00000 | 20160805 | OT | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
93436722 | 9343672 | 1 | I | GLIMEPIRIDE. | GLIMEPIRIDE | 1 | Unknown | 4 MG, DAILY | U | 0 | 4 | MG | |||||||
93436722 | 9343672 | 2 | I | IRBESARTAN. | IRBESARTAN | 1 | Unknown | 300 MG, DAILY | U | 0 | 300 | MG | |||||||
93436722 | 9343672 | 3 | PS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | 20 MG, DAILY | U | 200794 | 20 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
93436722 | 9343672 | 1 | Product used for unknown indication |
93436722 | 9343672 | 2 | Product used for unknown indication |
93436722 | 9343672 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
93436722 | 9343672 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
93436722 | 9343672 | Drug interaction | |
93436722 | 9343672 | Hyponatraemia | |
93436722 | 9343672 | Malaise |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |