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
126821151 12682115 1 I 20160518 20160811 20160824 20160824 EXP GB-MHRA-EYC 00140272 GB-TEVA-685525ACC TEVA 80.00 YR F Y 50.00000 KG 20160825 MD 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
126821151 12682115 1 PS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 THIS HAD NOT BEEN STOPPED PRIOR TO THE BLEED U 76999
126821151 12682115 2 SS IBRUTINIB IBRUTINIB 1 Oral U 0 560 MG
126821151 12682115 3 C CHLORAMBUCIL CHLORAMBUCIL 1 0
126821151 12682115 4 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
126821151 12682115 5 C PREDNISOLONE. PREDNISOLONE 1 0
126821151 12682115 6 C RITUXIMAB RITUXIMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126821151 12682115 1 Cerebrovascular accident
126821151 12682115 2 Mantle cell lymphoma refractory

Outcome of event

Event ID CASEID OUTC COD
126821151 12682115 DE
126821151 12682115 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126821151 12682115 Haemorrhage intracranial
126821151 12682115 Hemiparesis

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
126821151 12682115 2 20160517 20160518 0