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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5195462 | 6206067 | I | 5195462-9 | 20061221 | 20061230 | EXP | SE-ABBOTT-06P-150-0354055-00 | ABBOTT | F | Y | 20061230 | OT | SWEDEN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5195462 | 1007999571 | PS | KALETRA | 1 | ORAL | UNKNOWN | 021226 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5195462 | 1007999571 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
5195462 | OT |
Reactions reported
Event ID | PT |
---|---|
5195462 | PULMONARY EMBOLISM |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |