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
125281371 12528137 1 I 20151030 20160622 20160705 20160705 EXP AU-KADMON PHARMACEUTICALS, LLC-KAD201606-002333 KADMON 59.00 YR M Y 105.00000 KG 20160705 CN AU AU

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
125281371 12528137 1 PS RIBAVIRIN. RIBAVIRIN 1 Oral 76203 600 MG BID
125281371 12528137 2 SS RIBAVIRIN. RIBAVIRIN 1 76203
125281371 12528137 3 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 3 TABLETS IN THE MORNING AND 1 AT NIGHT 0 TABLET BID
125281371 12528137 4 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 0
125281371 12528137 5 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 ACCUHALER 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125281371 12528137 1 Hepatitis C
125281371 12528137 2 Hepatic cirrhosis
125281371 12528137 3 Hepatitis C
125281371 12528137 4 Hepatic cirrhosis
125281371 12528137 5 Asthma

Outcome of event

Event ID CASEID OUTC COD
125281371 12528137 DS
125281371 12528137 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125281371 12528137 Asthma
125281371 12528137 Cushing's syndrome
125281371 12528137 Drug interaction

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
125281371 12528137 1 20151008 20160101 0
125281371 12528137 3 20151008 20160101 0