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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124767263 | 12476726 | 3 | F | 20160307 | 20160706 | 20160617 | 20160713 | EXP | BR-ASTELLAS-2016US023083 | ASTELLAS | 13.00 | YR | M | Y | 0.00000 | 20160713 | CN | GB | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124767263 | 12476726 | 1 | PS | AMBISOME | AMPHOTERICIN B | 1 | Intravenous (not otherwise specified) | U | 005607 | 50740 | 400 | MG | INJECTION | QD | |||||
| 124767263 | 12476726 | 2 | C | VANCOMYCIN | VANCOMYCIN | 1 | Intravenous (not otherwise specified) | U | 0 | 800 | MG | FORMULATION UNKNOWN | TID | ||||||
| 124767263 | 12476726 | 3 | C | ANTAK | RANITIDINE HYDROCHLORIDE | 1 | Unknown | UNK UNK, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN | ||||||||
| 124767263 | 12476726 | 4 | C | VANCOMICINA | VANCOMYCIN | 1 | Unknown | UNK UNK, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN | ||||||||
| 124767263 | 12476726 | 5 | C | RANITIDINE. | RANITIDINE | 1 | Unknown | U | 0 | 50 | MG | INJECTION | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124767263 | 12476726 | 1 | Product used for unknown indication |
| 124767263 | 12476726 | 2 | Product used for unknown indication |
| 124767263 | 12476726 | 3 | Product used for unknown indication |
| 124767263 | 12476726 | 4 | Product used for unknown indication |
| 124767263 | 12476726 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124767263 | 12476726 | OT |
| 124767263 | 12476726 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124767263 | 12476726 | Headache | |
| 124767263 | 12476726 | Nausea | |
| 124767263 | 12476726 | Phlebitis | |
| 124767263 | 12476726 | Rash generalised | |
| 124767263 | 12476726 | Respiratory distress |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 124767263 | 12476726 | 1 | 20160307 | 20160329 | 0 | |
| 124767263 | 12476726 | 2 | 20160307 | 20160329 | 0 | |
| 124767263 | 12476726 | 5 | 20160307 | 20160329 | 0 |