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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5688846 | 6601749 | I | 5688846-3 | 20080319 | 20080325 | 20080331 | EXP | US-NOVOPROD-273415 | NOVOPROD | 55 | YR | M | Y | 20080331 | CN | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5688846 | 1009726609 | PS | NOVOLOG | 1 | SUBCUTANEOUS | 13 IU, UNK | UNKNOWN | 020986 | |||
5688846 | 1009726610 | C | NOVOLIN N | 1 | SUBCUTANEOUS | 4 IU, UNK | 019959 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5688846 | 1009726609 | TYPE 1 DIABETES MELLITUS |
5688846 | 1009726610 | TYPE 1 DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
5688846 | LT |
Reactions reported
Event ID | PT |
---|---|
5688846 | BLOOD GLUCOSE DECREASED |
5688846 | CONTUSION |
5688846 | FALL |
5688846 | LOSS OF CONSCIOUSNESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |