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
124701213 12470121 3 F 20160915 20160616 20160923 EXP NL-ROCHE-1775253 ROCHE 0.00 F Y 0.00000 20160923 OT NL NL

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
124701213 12470121 1 PS LUCENTIS RANIBIZUMAB 1 Unknown U 125156 SOLUTION FOR INJECTION
124701213 12470121 2 SS LUCENTIS RANIBIZUMAB 1 Unknown 1 DF, QMO U 125156 1 DF SOLUTION FOR INJECTION /month
124701213 12470121 3 C ISOPTIN VERAPAMIL HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124701213 12470121 1 Neovascular age-related macular degeneration
124701213 12470121 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124701213 12470121 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124701213 12470121 Abdominal pain
124701213 12470121 Cyst
124701213 12470121 Eye disorder
124701213 12470121 Gastrointestinal disorder
124701213 12470121 Glaucoma
124701213 12470121 Inappropriate schedule of drug administration
124701213 12470121 Intraocular melanoma
124701213 12470121 Lacrimation increased
124701213 12470121 Macular degeneration
124701213 12470121 Retinal disorder
124701213 12470121 Syringe issue
124701213 12470121 Vision blurred
124701213 12470121 Visual acuity reduced

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
124701213 12470121 1 2013 0
124701213 12470121 2 2014 0