The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
121816836 12181683 6 F 20160105 20160803 20160315 20160810 PER PHHY2016US032585 NOVARTIS 65.67 YR F Y 63.00000 KG 20160810 CN US US

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
121816836 12181683 1 PS SIMULECT BASILIXIMAB 1 Intravenous (not otherwise specified) 20 MG, (ON DAY 0 AND DAY 4) 103764 20 MG
121816836 12181683 2 SS SIMULECT BASILIXIMAB 1 103764
121816836 12181683 3 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Oral 1000 MG, BID 44000 MG 0 1000 MG BID
121816836 12181683 4 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Oral 750 MG, BID 44000 MG 0 750 MG BID
121816836 12181683 5 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Oral 500 MG, BID 44000 MG 0 500 MG BID
121816836 12181683 6 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Oral 250 MG, BID 44000 MG 0 250 MG BID
121816836 12181683 7 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Unknown UNK 44000 MG 0
121816836 12181683 8 SS GEODON ZIPRASIDONE HYDROCHLORIDEIPRASIDONE MESYLATE 1 Oral 80 MG, QD Y 0 80 MG QD
121816836 12181683 9 SS GEODON ZIPRASIDONE HYDROCHLORIDEIPRASIDONE MESYLATE 1 Oral 40 MG, QD Y 0 40 MG QD
121816836 12181683 10 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121816836 12181683 1 Renal transplant
121816836 12181683 2 Immunosuppressant drug therapy
121816836 12181683 3 Renal transplant
121816836 12181683 4 Immunosuppressant drug therapy
121816836 12181683 8 Schizophrenia
121816836 12181683 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121816836 12181683 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121816836 12181683 Agranulocytosis
121816836 12181683 Leukopenia

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
121816836 12181683 1 20131003 20131007 0
121816836 12181683 4 20140708 0
121816836 12181683 5 20140923 0
121816836 12181683 6 20150825 20151120 0
121816836 12181683 9 20151214 0