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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125442081 | 12544208 | 1 | I | 20160622 | 20160705 | 20160711 | 20160711 | EXP | GB-009507513-1606GBR012775 | GB-GLENMARK GENERICS (EUROPE) LTD.-2016GMK023564 | GLENMARK | 0.00 | Y | 0.00000 | 20160711 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125442081 | 12544208 | 1 | PS | EZETIMIBE. | EZETIMIBE | 1 | Oral | UNK | U | 78560 | TABLET | ||||||||
125442081 | 12544208 | 2 | SS | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | UNK | U | 0 | |||||||||
125442081 | 12544208 | 3 | SS | CLEXANE | ENOXAPARIN SODIUM | 1 | Unknown | UNK | U | 0 | |||||||||
125442081 | 12544208 | 4 | SS | INSULIN | INSULIN NOS | 1 | Unknown | UNK | U | 0 | |||||||||
125442081 | 12544208 | 5 | SS | METRONIDAZOLE. | METRONIDAZOLE | 1 | Unknown | UNK | U | 0 | |||||||||
125442081 | 12544208 | 6 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | UNK | U | 0 | |||||||||
125442081 | 12544208 | 7 | SS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125442081 | 12544208 | 1 | Product used for unknown indication |
125442081 | 12544208 | 2 | Product used for unknown indication |
125442081 | 12544208 | 3 | Product used for unknown indication |
125442081 | 12544208 | 4 | Product used for unknown indication |
125442081 | 12544208 | 5 | Product used for unknown indication |
125442081 | 12544208 | 6 | Product used for unknown indication |
125442081 | 12544208 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125442081 | 12544208 | OT |
125442081 | 12544208 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125442081 | 12544208 | Acute kidney injury |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |