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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4915190 | 5989984 | I | 4915190-1 | 20050814 | 20060216 | DIR | F | N | 20051128 | PH | N | Y | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4915190 | 1006947756 | PS | LANTUS | 1 | UNKNOWN | UNKNOWN - PRIOR TO ADMISSION | Y | D | |||
4915190 | 1006969667 | SS | HUMALOG | 1 | UNKNOWN | UNKNOWN - PRIOR TO ADMISSION | Y | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4915190 | 1006947756 | DIABETES MELLITUS |
4915190 | 1006969667 | DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
4915190 | HO |
Reactions reported
Event ID | PT |
---|---|
4915190 | DEPRESSED LEVEL OF CONSCIOUSNESS |
4915190 | DYSARTHRIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |