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
126258261 12625826 1 I 201603 20160401 20160805 20160805 PER US-ABBVIE-16P-163-1597001-00 ABBVIE 23.00 YR F Y 0.00000 20160805 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
126258261 12625826 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619 TABLET
126258261 12625826 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 0 1000 MG TABLET
126258261 12625826 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 0 TABLET
126258261 12625826 4 C PROZAC FLUOXETINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126258261 12625826 1 Chronic hepatitis C
126258261 12625826 2 Chronic hepatitis C
126258261 12625826 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126258261 12625826 Bilirubin conjugated abnormal
126258261 12625826 Blood bilirubin decreased
126258261 12625826 Blood bilirubin increased
126258261 12625826 Chromaturia
126258261 12625826 Haemoglobin decreased
126258261 12625826 Jaundice
126258261 12625826 Ocular icterus

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
126258261 12625826 1 20160318 0
126258261 12625826 2 20160318 0
126258261 12625826 3 201604 0