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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125252761 | 12525276 | 1 | I | 20160627 | 20160704 | 20160704 | PER | US-ELI_LILLY_AND_COMPANY-US201606011022 | ELI LILLY AND CO | 0.00 | F | Y | 0.00000 | 20160704 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125252761 | 12525276 | 1 | PS | HUMULIN 70/30 | INSULIN HUMAN | 1 | Unknown | UNK, UNKNOWN | U | U | C517663C | 18780 | INJECTION | ||||||
125252761 | 12525276 | 2 | C | ATORVASTATIN | ATORVASTATIN | 1 | 80 MG, UNKNOWN | U | 0 | 80 | MG | ||||||||
125252761 | 12525276 | 3 | C | LISINOPRIL. | LISINOPRIL | 1 | 20 MG, UNKNOWN | U | 0 | 20 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125252761 | 12525276 | 1 | Diabetes mellitus |
125252761 | 12525276 | 2 | Product used for unknown indication |
125252761 | 12525276 | 3 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125252761 | 12525276 | Blood glucose increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |