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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125617731 | 12561773 | 1 | I | 20160619 | 20160706 | 20160715 | 20160715 | EXP | US-NOVOPROD-500667 | NOVO NORDISK | 41.00 | YR | A | F | Y | 107.94000 | KG | 20160715 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125617731 | 12561773 | 1 | PS | NOVOLOG | INSULIN ASPART | 1 | Subcutaneous | SLIDING SCALE, TID | Y | EZF0449 | 20986 | SOLUTION FOR INJECTION | TID | ||||||
125617731 | 12561773 | 2 | SS | LANTUS | INSULIN GLARGINE | 1 | Subcutaneous | 50 U, BID | Y | UNKNOWN | 0 | 50 | DF | BID | |||||
125617731 | 12561773 | 3 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | UNKNOWN | 0 | ||||||||||
125617731 | 12561773 | 4 | C | LOSARTAN. | LOSARTAN | 1 | UNK | UNKNOWN | 0 | ||||||||||
125617731 | 12561773 | 5 | C | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | UNK | UNKNOWN | 0 | ||||||||||
125617731 | 12561773 | 6 | C | ATORVASTATIN | ATORVASTATIN | 1 | UNK | UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125617731 | 12561773 | 1 | Type 2 diabetes mellitus |
125617731 | 12561773 | 2 | Type 2 diabetes mellitus |
125617731 | 12561773 | 3 | Product used for unknown indication |
125617731 | 12561773 | 4 | Product used for unknown indication |
125617731 | 12561773 | 5 | Product used for unknown indication |
125617731 | 12561773 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125617731 | 12561773 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125617731 | 12561773 | Abdominal pain lower | |
125617731 | 12561773 | Blood glucose increased | |
125617731 | 12561773 | Pancreatitis | |
125617731 | 12561773 | Product quality issue |
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 |
---|---|---|---|---|---|---|
125617731 | 12561773 | 1 | 2014 | 20160706 | 0 | |
125617731 | 12561773 | 2 | 2014 | 20160706 | 0 |