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
124896572 12489657 2 F 201606 20160715 20160622 20160726 EXP FR-GILEAD-2016-0218471 GILEAD 83.00 YR E F Y 0.00000 20160726 MD FR FR

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
124896572 12489657 1 PS ZYDELIG IDELALISIB 1 Oral UNK Y 205858 TABLET
124896572 12489657 2 SS RITUXIMAB RITUXIMAB 1 Intravenous (not otherwise specified) UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124896572 12489657 1 Chronic lymphocytic leukaemia
124896572 12489657 2 Chronic lymphocytic leukaemia

Outcome of event

Event ID CASEID OUTC COD
124896572 12489657 HO
124896572 12489657 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124896572 12489657 Hyponatraemia
124896572 12489657 Interstitial lung disease
124896572 12489657 Neutropenia
124896572 12489657 Urinary retention

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
124896572 12489657 1 201506 201606 0
124896572 12489657 2 2015 0