Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125760043 | 12576004 | 3 | F | 20160815 | 20160720 | 20160824 | EXP | CN-ASTELLAS-2016US027869 | ASTELLAS | 5.00 | YR | Y | 0.00000 | 20160824 | CN | GB | CN |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125760043 | 12576004 | 1 | PS | AMBISOME | AMPHOTERICIN B | 1 | Intravenous (not otherwise specified) | 50740 | 65 | MG/KG | INJECTION | ||||||||
| 125760043 | 12576004 | 2 | SS | AMBISOME | AMPHOTERICIN B | 1 | Respiratory (inhalation) | 50740 | 65 | MG/KG | INJECTION | ||||||||
| 125760043 | 12576004 | 3 | C | ITRACONAZOLE. | ITRACONAZOLE | 1 | Unknown | UNK UNK, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125760043 | 12576004 | 1 | Bronchopulmonary aspergillosis |
| 125760043 | 12576004 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125760043 | 12576004 | OT |
| 125760043 | 12576004 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125760043 | 12576004 | Drug ineffective | |
| 125760043 | 12576004 | Off label use |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |