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
116173064 11617306 4 F 2015 20160903 20151009 20160913 EXP US-JNJFOC-20151005589 PHARMACYCLICS 72.51 YR E F Y 0.00000 20160913 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
116173064 11617306 1 SS IMBRUVICA IBRUTINIB 1 Oral U U L0501370A1 0 560 MG CAPSULE QD
116173064 11617306 2 PS IMBRUVICA IBRUTINIB 1 Oral U U L0501370A1 205552 560 MG CAPSULE QD
116173064 11617306 3 SS DILTIAZEM. DILTIAZEM 1 Y 0
116173064 11617306 4 C TELMISARTAN. TELMISARTAN 1 0
116173064 11617306 5 C MAGNESIUM MAGNESIUM 1 0
116173064 11617306 6 C OMEGA 3 OMEGA-3 FATTY ACIDS 1 0
116173064 11617306 7 C PROBIOTIC PROBIOTICS NOS 1 0
116173064 11617306 8 C VITAMIN D3 CHOLECALCIFEROL 1 0
116173064 11617306 9 C COENZYME Q10 UBIDECARENONE 1 0
116173064 11617306 10 C CAMELLIA SINENSIS GREEN TEA LEAF 1 0
116173064 11617306 11 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 0 UNSPECIFIED
116173064 11617306 12 C COLACE DOCUSATE SODIUM 1 0
116173064 11617306 13 C PROTONIX PANTOPRAZOLE SODIUM 1 0
116173064 11617306 14 C LYRICA PREGABALIN 1 0
116173064 11617306 15 C ROBAXIN METHOCARBAMOL 1 0
116173064 11617306 16 C HYDROCODONE HYDROCODONE 1 0
116173064 11617306 17 C BYSTOLIC NEBIVOLOL HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116173064 11617306 1 Non-Hodgkin's lymphoma
116173064 11617306 2 Chronic lymphocytic leukaemia
116173064 11617306 3 Product used for unknown indication
116173064 11617306 4 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
116173064 11617306 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116173064 11617306 Asthenia
116173064 11617306 Back pain
116173064 11617306 Blood pressure increased
116173064 11617306 Blood sodium decreased
116173064 11617306 Fatigue
116173064 11617306 Hypoaesthesia
116173064 11617306 Paraesthesia
116173064 11617306 Pruritus
116173064 11617306 Weight increased

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
116173064 11617306 1 20150109 0
116173064 11617306 2 20150109 0
116173064 11617306 3 20150904 20150927 0
116173064 11617306 4 2014 0