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
126792071 12679207 1 I 20160518 20160811 20160824 20160824 EXP GB-MHRA-ADR 23491601 GB-ACCORD-043303 ACCORD 80.00 YR F Y 50.00000 KG 20160824 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
126792071 12679207 1 PS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 202925
126792071 12679207 2 SS IBRUTINIB IBRUTINIB 1 Oral 0 560 MG
126792071 12679207 3 C CHLORAMBUCIL CHLORAMBUCIL 1 0
126792071 12679207 4 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
126792071 12679207 5 C PREDNISOLONE. PREDNISOLONE 1 0
126792071 12679207 6 C RITUXIMAB RITUXIMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126792071 12679207 1 Cerebrovascular accident
126792071 12679207 2 Mantle cell lymphoma refractory

Outcome of event

Event ID CASEID OUTC COD
126792071 12679207 OT
126792071 12679207 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126792071 12679207 Haemorrhage intracranial
126792071 12679207 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
126792071 12679207 2 20160517 20160518 0