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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5195467 | 6206072 | I | 5195467-8 | 20061220 | 20061230 | EXP | FR-ABBOTT-06P-056-0353938-00 | ABBOTT | Y | 20061230 | MD | FRANCE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5195467 | 1007999594 | PS | KALETRA | 1 | ORAL | UNKNOWN | 021226 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5195467 | 1007999594 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
5195467 | OT |
Reactions reported
Event ID | PT |
---|---|
5195467 | RHABDOMYOLYSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |