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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124960672 | 12496067 | 2 | F | 2009 | 20160628 | 20160624 | 20160706 | EXP | CN-ELI_LILLY_AND_COMPANY-CN201606007801 | ELI LILLY AND CO | 0.00 | F | Y | 62.00000 | KG | 20160706 | CN | CN | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124960672 | 12496067 | 1 | PS | HUMULIN R | INSULIN HUMAN | 1 | Unknown | UNK, UNKNOWN | U | U | 18780 | INJECTION | |||||||
124960672 | 12496067 | 2 | SS | HUMULIN R | INSULIN HUMAN | 1 | Subcutaneous | 8 U, EACH MORNING | U | U | 18780 | 8 | IU | INJECTION | QD | ||||
124960672 | 12496067 | 3 | SS | HUMULIN R | INSULIN HUMAN | 1 | Subcutaneous | 8 U, AT NOON | U | U | 18780 | 8 | IU | INJECTION | QD | ||||
124960672 | 12496067 | 4 | SS | HUMULIN R | INSULIN HUMAN | 1 | Subcutaneous | 8 U, AT NOON | U | U | 18780 | 8 | IU | INJECTION | QD | ||||
124960672 | 12496067 | 5 | SS | HUMULIN N | INSULIN HUMAN | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | INJECTION | |||||||
124960672 | 12496067 | 6 | SS | HUMULIN N | INSULIN HUMAN | 1 | Subcutaneous | 17 U, EACH EVENING | U | U | 0 | 17 | IU | INJECTION | QD | ||||
124960672 | 12496067 | 7 | C | ACARBOSE. | ACARBOSE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
124960672 | 12496067 | 8 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
124960672 | 12496067 | 9 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
124960672 | 12496067 | 10 | C | CONCOR | BISOPROLOL FUMARATE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
124960672 | 12496067 | 11 | C | ANBOL | 2 | Unknown | UNK, UNKNOWN | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124960672 | 12496067 | 1 | Diabetes mellitus |
124960672 | 12496067 | 5 | Diabetes mellitus |
124960672 | 12496067 | 7 | Product used for unknown indication |
124960672 | 12496067 | 8 | Product used for unknown indication |
124960672 | 12496067 | 9 | Product used for unknown indication |
124960672 | 12496067 | 10 | Product used for unknown indication |
124960672 | 12496067 | 11 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124960672 | 12496067 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124960672 | 12496067 | Blood glucose abnormal | |
124960672 | 12496067 | Blood glucose decreased | |
124960672 | 12496067 | Blood glucose increased | |
124960672 | 12496067 | Diabetic ketoacidosis | |
124960672 | 12496067 | Ear disorder | |
124960672 | 12496067 | Peripheral swelling | |
124960672 | 12496067 | Visual acuity reduced |
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 |
---|---|---|---|---|---|---|
124960672 | 12496067 | 1 | 2009 | 0 | ||
124960672 | 12496067 | 5 | 2009 | 0 |