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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126493141 | 12649314 | 1 | I | 20160803 | 20160812 | 20160812 | PER | US-ELI_LILLY_AND_COMPANY-US201608004014 | ELI LILLY AND CO | 64.00 | YR | M | Y | 0.00000 | 20160812 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126493141 | 12649314 | 1 | PS | HUMULIN 70/30 | INSULIN HUMAN | 1 | Unknown | UNK UNK, UNKNOWN | U | U | 18780 | INJECTION | |||||||
126493141 | 12649314 | 2 | SS | HUMULIN 70/30 | INSULIN HUMAN | 1 | Unknown | 50 U, BID | U | U | 18780 | 50 | IU | INJECTION | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126493141 | 12649314 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126493141 | 12649314 | HO |
126493141 | 12649314 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126493141 | 12649314 | Blood glucose increased | |
126493141 | 12649314 | Hypoglycaemia | |
126493141 | 12649314 | Loss of consciousness |
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 |
---|---|---|---|---|---|---|
126493141 | 12649314 | 2 | 20160701 | 0 |