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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126209471 | 12620947 | 1 | I | 20160722 | 20160804 | 20160804 | EXP | PHFR2016GB006206 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160804 | CN | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126209471 | 12620947 | 1 | PS | DEFEROXAMINE | DEFEROXAMINEDEFEROXAMINE MESYLATE | 1 | Unknown | 2G IN 40ML (0.9% BP) SODIUM CHLORIDE 5 TIMES A WEEK | C132237AA | 16267 | |||||||||
126209471 | 12620947 | 2 | SS | SODIUM CHLORIDE. | SODIUM CHLORIDE | 1 | Unknown | 2G DESFERRIOXAMINE IN 40 ML (0.9% BP) SODIUM CHLORIDE 5 TIMES PER WEEK | U | 14L22E9U | 0 | ||||||||
126209471 | 12620947 | 3 | SS | WATER FOR INJECTION | WATER | 1 | Unknown | UNK | U | 15L21T1D | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126209471 | 12620947 | 1 | Product used for unknown indication |
126209471 | 12620947 | 2 | Product used for unknown indication |
126209471 | 12620947 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126209471 | 12620947 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126209471 | 12620947 | Pyrexia | |
126209471 | 12620947 | Viral infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |