Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4430567 | 4196731 | I | 4430567-9 | 20040803 | 20040818 | EXP | 238423 | NOVO NORDISK PHARMACEUTICALS INC. | F | N | 20040812 | CN |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4430567 | 1005132455 | PS | MIXTARD HUMAN 70/30 | 1 | U | U | 19991 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4430567 | 1005132455 | ILL-DEFINED DISORDER |
Outcome of event
Event ID | OUTC COD |
---|---|
4430567 | HO |
Reactions reported
Event ID | PT |
---|---|
4430567 | GASTROINTESTINAL DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4430567 | CSM |
4430567 | FGN |
4430567 | OTH |
Therapies reported
no results found |