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
111735395 11173539 5 F 20150225 20160823 20150609 20160824 EXP CA-ROCHE-1589580 ROCHE 84.53 YR F Y 0.00000 20160824 CN CA CA

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
111735395 11173539 1 PS LUCENTIS RANIBIZUMAB 1 Other 10 MG/ML 125156 SOLUTION FOR INJECTION
111735395 11173539 2 SS AVASTIN BEVACIZUMAB 1 Intravenous (not otherwise specified) U 125085

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111735395 11173539 1 Neovascular age-related macular degeneration
111735395 11173539 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
111735395 11173539 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111735395 11173539 Drug interaction
111735395 11173539 Eye contusion
111735395 11173539 Eye discharge
111735395 11173539 Eye infection
111735395 11173539 Eye swelling
111735395 11173539 Fall
111735395 11173539 Iodine allergy
111735395 11173539 Neck pain
111735395 11173539 Ocular hyperaemia
111735395 11173539 Photophobia
111735395 11173539 Swelling face
111735395 11173539 Visual acuity reduced
111735395 11173539 Visual impairment

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found