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
125627211 12562721 1 I 20160707 20160715 20160715 EXP US-KADMON PHARMACEUTICALS, LLC-KAD201607-002592 KADMON 0.00 F Y 0.00000 20160715 MD 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
125627211 12562721 1 PS RIBAVIRIN. RIBAVIRIN 1 Oral TABLET 77456 TABLET
125627211 12562721 2 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral TABLET 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125627211 12562721 1 Hepatitis C
125627211 12562721 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125627211 12562721 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125627211 12562721 Abdominal pain lower
125627211 12562721 Chest pain
125627211 12562721 Diarrhoea
125627211 12562721 Dry mouth
125627211 12562721 Dyspnoea
125627211 12562721 Flatulence
125627211 12562721 Hyperhidrosis

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
125627211 12562721 1 20160503 0
125627211 12562721 2 20160503 0