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
124540804 12454080 4 F 20151230 20160721 20160610 20160808 EXP TW-ROCHE-1759730 ROCHE 82.22 YR M Y 54.00000 KG 20160808 MD TW TW

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
124540804 12454080 1 PS Ranibizumab RANIBIZUMAB 1 Other 10 MG/ML 125156 .5 MG SOLUTION FOR INJECTION
124540804 12454080 2 SS Ranibizumab RANIBIZUMAB 1 Other RIGHT EYE 125156 .5 MG SOLUTION FOR INJECTION
124540804 12454080 3 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown Y 0 .2 MG
124540804 12454080 4 C FLUOROMETHOLONE. FLUOROMETHOLONE 1 Unknown Y 0 .02 MG
124540804 12454080 5 C SULFAMETHOXAZOLE SULFAMETHOXAZOLE 1 Unknown Y 0 8 MG
124540804 12454080 6 C TOBRAMYCIN. TOBRAMYCIN 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124540804 12454080 1 Age-related macular degeneration
124540804 12454080 3 Prophylaxis
124540804 12454080 4 Conjunctival haemorrhage
124540804 12454080 5 Prophylaxis
124540804 12454080 6 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
124540804 12454080 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124540804 12454080 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
124540804 12454080 1 20150527 20150527 0
124540804 12454080 2 20151202 20151202 0
124540804 12454080 3 20151102 20160102 0
124540804 12454080 4 20151202 20160102 0
124540804 12454080 5 20150902 20160427 0
124540804 12454080 6 20151102 20160102 0