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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7582991 | 8016560 | I | 7582991-3 | 20110524 | 20110630 | EXP | US-SANOFI-AVENTIS-2011SA040440 | SANOFI-AVENTIS | YR | Y | 20110630 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7582991 | 1016902954 | SS | SOLOSTAR | 2 | 0F572A | ||||||
7582991 | 1016902955 | PS | LANTUS | 1 | PARENTERAL | 0F572A | 021081 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7582991 | 1016902954 | PRODUCT USED FOR UNKNOWN INDICATION |
7582991 | 1016902955 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
7582991 | OT |
Reactions reported
Event ID | PT |
---|---|
7582991 | DEVICE MALFUNCTION |
7582991 | PRODUCT QUALITY ISSUE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |