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
127154102 12715410 2 F 20150728 20160921 20160906 20160926 EXP FR-ROCHE-1618095 ROCHE 56.19 YR M Y 70.10000 KG 20160926 MD FR FR

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
127154102 12715410 1 PS Ranibizumab RANIBIZUMAB 1 Other 125156 SOLUTION FOR INJECTION
127154102 12715410 2 SS Ranibizumab RANIBIZUMAB 1 Other 125156 SOLUTION FOR INJECTION
127154102 12715410 3 SS Ranibizumab RANIBIZUMAB 1 Other 125156 SOLUTION FOR INJECTION
127154102 12715410 4 C PRETERAX INDAPAMIDEPERINDOPRIL 1 Oral 0 2.5 MG QD
127154102 12715410 5 C DIFFU K POTASSIUM CHLORIDE 1 Unknown U 0
127154102 12715410 6 C PARACETAMOL ACETAMINOPHEN 1 Unknown U 0
127154102 12715410 7 C AZARGA BRINZOLAMIDETIMOLOL MALEATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127154102 12715410 1 Eye disorder
127154102 12715410 4 Hypertension
127154102 12715410 5 Glaucoma
127154102 12715410 6 Product used for unknown indication
127154102 12715410 7 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
127154102 12715410 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127154102 12715410 Ocular hypertension

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
127154102 12715410 1 20150519 0
127154102 12715410 2 20150728 0
127154102 12715410 3 20151207 0
127154102 12715410 4 2007 0
127154102 12715410 5 201510 20160215 0
127154102 12715410 6 201602 20160215 0
127154102 12715410 7 201512 20160215 0