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
125281441 12528144 1 I 20160526 20160624 20160705 20160705 EXP US-KADMON PHARMACEUTICALS, LLC-KAD201606-002369 KADMON 25.44 YR M Y 81.65000 KG 20160705 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
125281441 12528144 1 PS RIBAVIRIN. RIBAVIRIN 1 Oral TABLET Y 77456 600 MG TABLET
125281441 12528144 2 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral TABLET Y 0 TABLET
125281441 12528144 3 SS ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Y 0
125281441 12528144 4 C METHADONE METHADONE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125281441 12528144 1 Hepatitis C
125281441 12528144 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125281441 12528144 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125281441 12528144 Asthenia
125281441 12528144 Drug ineffective
125281441 12528144 Dyspnoea
125281441 12528144 Epilepsy
125281441 12528144 Feeling abnormal
125281441 12528144 Gait disturbance
125281441 12528144 Headache
125281441 12528144 Heart rate increased
125281441 12528144 Hyperhidrosis
125281441 12528144 Hypophagia
125281441 12528144 Migraine
125281441 12528144 Nausea
125281441 12528144 Vomiting

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
125281441 12528144 1 20160526 20160607 0
125281441 12528144 2 20160526 20160607 0