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
126712511 12671251 1 I 20160518 20160811 20160822 20160822 EXP GB-MHRA-EYC 00140272 GB-DRREDDYS-GER/UKI/16/0082401 DR REDDYS 80.00 YR F Y 50.00000 KG 20160822 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
126712511 12671251 1 PS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 THIS HAD NOT BEEN STOPPED PRIOR TO THE BLEED U UNKNOWN 76273
126712511 12671251 2 SS IBRUTINIB IBRUTINIB 1 Oral U 0 560 MG
126712511 12671251 3 C CHLORAMBUCIL CHLORAMBUCIL 1 0
126712511 12671251 4 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
126712511 12671251 5 C PREDNISOLONE. PREDNISOLONE 1 0
126712511 12671251 6 C RITUXIMAB RITUXIMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712511 12671251 1 Cerebrovascular accident
126712511 12671251 2 Mantle cell lymphoma refractory
126712511 12671251 3 Product used for unknown indication
126712511 12671251 4 Product used for unknown indication
126712511 12671251 5 Product used for unknown indication
126712511 12671251 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126712511 12671251 DE
126712511 12671251 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712511 12671251 Haemorrhage intracranial
126712511 12671251 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
126712511 12671251 2 20160517 20160518 0