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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6194992 | 6997728 | I | 6194992-0 | 20090511 | 20090519 | EXP | A0783522A | GLAXOSMITHKLINE | Y | 20090519 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6194992 | 1011592773 | PS | LOVAZA | 1 | UNKNOWN | UNKNOWN | 021654 | ||||
6194992 | 1011592774 | C | NO CONCURRENT MEDICATION | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6194992 | 1011592773 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6194992 | OT |
Reactions reported
Event ID | PT |
---|---|
6194992 | ALANINE AMINOTRANSFERASE INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |