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
125756511 12575651 1 I 20160311 20160713 20160720 20160720 EXP US-KADMON PHARMACEUTICALS, LLC-KAD201607-002614 KADMON 75.00 YR F Y 42.63000 KG 20160720 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
125756511 12575651 1 PS RIBAVIRIN. RIBAVIRIN 1 Oral Y 76203 100 MG TID
125756511 12575651 2 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 12.5/75/50/25 MG Y 0 BID
125756511 12575651 3 C CALCIUM ACETATE. CALCIUM ACETATE 1 0
125756511 12575651 4 C AMLODIPINE AMLODIPINE BESYLATE 1 0
125756511 12575651 5 C COZAAR LOSARTAN POTASSIUM 1 0
125756511 12575651 6 C COREG CARVEDILOL 1 0
125756511 12575651 7 C Calcitrol CALCITRIOL 1 0
125756511 12575651 8 C VITAMIN D2 ERGOCALCIFEROL 1 0
125756511 12575651 9 C RITONAVIR. RITONAVIR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125756511 12575651 1 Hepatitis C
125756511 12575651 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125756511 12575651 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125756511 12575651 Dizziness
125756511 12575651 Hypotension

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
125756511 12575651 1 20150910 20151103 0
125756511 12575651 2 20150910 20151103 0