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
125217761 12521776 1 I 20160623 20160701 20160701 EXP US-KADMON PHARMACEUTICALS, LLC-KAD201606-002334 KADMON 0.00 M Y 0.00000 20160701 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
125217761 12521776 1 PS RIBAVIRIN. RIBAVIRIN 1 Oral Y 77456
125217761 12521776 2 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral TABLET Y 0 TABLET
125217761 12521776 3 C LOSARTAN. LOSARTAN 1 0
125217761 12521776 4 C METOPROLOL. METOPROLOL 1 0
125217761 12521776 5 C AMLODIPINE AMLODIPINE BESYLATE 1 0
125217761 12521776 6 C Oxycodone OXYCODONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125217761 12521776 1 Hepatitis C
125217761 12521776 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125217761 12521776 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125217761 12521776 Blood creatinine increased
125217761 12521776 Glomerular filtration rate decreased
125217761 12521776 Rash

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found