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
119350524 11935052 4 F 20141201 20160823 20160121 20160829 EXP PHHY2015CA030788 SANDOZ 84.24 YR F Y 0.00000 20160829 OT 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
119350524 11935052 1 SS LUCENTIS RANIBIZUMAB 1 Intraocular 0.5 MG, UNK 0 .5 MG INJECTION
119350524 11935052 2 SS LUCENTIS RANIBIZUMAB 1 Intraocular 0.5 MG, UNK 0 .5 MG INJECTION
119350524 11935052 3 PS WARFARIN WARFARIN 1 Unknown U 40196

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119350524 11935052 1 Age-related macular degeneration
119350524 11935052 2 Choroidal neovascularisation
119350524 11935052 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119350524 11935052 OT
119350524 11935052 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119350524 11935052 Atrial fibrillation
119350524 11935052 Blood pressure diastolic increased
119350524 11935052 Blood pressure increased
119350524 11935052 Blood pressure systolic increased
119350524 11935052 Cardiac failure congestive
119350524 11935052 Fall
119350524 11935052 International normalised ratio abnormal
119350524 11935052 Lacrimation increased
119350524 11935052 Leukocytosis
119350524 11935052 Musculoskeletal chest pain
119350524 11935052 Pulmonary mass
119350524 11935052 Pyrexia

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
119350524 11935052 1 20140604 0
119350524 11935052 2 20160608 20160608 0