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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7023586 | 7621313 | I | 7023586-X | 20100818 | 20100930 | DIR | -1 | YR | F | N | 196 | LBS | 20100917 | N | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7023586 | 1014815180 | PS | MEPRON | 1 | Y |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7023586 | 1014815180 | BABESIOSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
7023586 | OT |
Reactions reported
Event ID | PT |
---|---|
7023586 | HEPATIC ENZYME INCREASED |
7023586 | NAUSEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |