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
119290475 11929047 5 F 20160129 20160817 20160120 20160824 EXP US-ROCHE-1695894 ROCHE 17.04 YR F Y 46.00000 KG 20160824 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
119290475 11929047 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 270 UG /wk
119290475 11929047 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 270 MG /wk
119290475 11929047 3 C FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 Oral 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119290475 11929047 1 Malignant melanoma
119290475 11929047 3 Depression

Outcome of event

Event ID CASEID OUTC COD
119290475 11929047 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119290475 11929047 Autoimmune thyroiditis
119290475 11929047 Hypothyroidism
119290475 11929047 Menstruation delayed
119290475 11929047 Mental disorder
119290475 11929047 Panic attack
119290475 11929047 Suicidal ideation

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
119290475 11929047 1 20151117 201607 0
119290475 11929047 2 20151211 0
119290475 11929047 3 201601 0