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
126962382 12696238 2 F 20160905 20160829 20160907 EXP DE-ROCHE-1821511 ROCHE PRIVACY. ANALYSIS OF CARDIOVASCULAR DISEASES AFTER THE UPLOAD PHASE WITH INTRAVITREAL RANIBIZUMAB AND BEVACIZUMAB IN PATIENTS WITH EXUDATIVE AGE- RELATED MACULAR DEGENERATION. DER OPHTHALMOLOGE 2016 ;:-. 0.00 E M Y 0.00000 20160907 OT DE DE

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
126962382 12696238 1 PS LUCENTIS RANIBIZUMAB 1 Intraocular UNK 125156 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126962382 12696238 1 Neovascular age-related macular degeneration

Outcome of event

Event ID CASEID OUTC COD
126962382 12696238 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126962382 12696238 Death

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

no results found

Therapies reported

no results found