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
127233411 12723341 1 I 20160901 20160908 20160908 EXP US-ROCHE-1825022 ROCHE 0.00 M Y 0.00000 20160908 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
127233411 12723341 1 PS LUCENTIS RANIBIZUMAB 1 Other U 125156 .5 MG SOLUTION FOR INJECTION /month
127233411 12723341 2 SS VALIUM DIAZEPAM 1 Intravenous (not otherwise specified) U 13263 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127233411 12723341 1 Neovascular age-related macular degeneration
127233411 12723341 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127233411 12723341 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127233411 12723341 Balance disorder
127233411 12723341 Depressed mood
127233411 12723341 Dizziness
127233411 12723341 Fall
127233411 12723341 Feeling hot
127233411 12723341 Gait disturbance
127233411 12723341 Hand fracture
127233411 12723341 Headache
127233411 12723341 Ill-defined disorder
127233411 12723341 Nausea
127233411 12723341 Nervousness
127233411 12723341 Respiratory arrest
127233411 12723341 Vision blurred

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
127233411 12723341 1 20160809 0