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
106384184 10638418 4 F 20140401 20160920 20141208 20160922 EXP IT-JNJFOC-20141118992 JANSSEN 89.92 YR E F Y 56.00000 KG 20160922 MD IT IT

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
106384184 10638418 1 PS ITRACONAZOLE. ITRACONAZOLE 1 Oral Y N 20083 100 MG UNSPECIFIED
106384184 10638418 2 SS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral Y 0 220 MG CAPSULE, HARD
106384184 10638418 3 C LASIX FUROSEMIDE 1 Oral D 0 50 MG TABLETS
106384184 10638418 4 C KANRENOL CANRENOATE POTASSIUM 1 Oral D 0 25 MG TABLETS
106384184 10638418 5 C PANTORC PANTOPRAZOLE SODIUM 1 Oral D 0 40 MG TABLETS
106384184 10638418 6 C SIMVASTATIN. SIMVASTATIN 1 Oral D 0 20 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106384184 10638418 1 Onychomycosis
106384184 10638418 2 Atrial fibrillation
106384184 10638418 3 Product used for unknown indication
106384184 10638418 4 Product used for unknown indication
106384184 10638418 5 Product used for unknown indication
106384184 10638418 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
106384184 10638418 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106384184 10638418 Muscle haemorrhage

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
106384184 10638418 1 20140401 20150506 0
106384184 10638418 2 20140207 20140727 0