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
95109628 9510962 8 F 201210 20160715 20130910 20160720 EXP BR-ROCHE-1272292 ROCHE 37.93 YR M Y 52.00000 KG 20160720 MD BR BR

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
95109628 9510962 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 SOLUTION FOR INFUSION
95109628 9510962 2 C PREDNISONE. PREDNISONE 1 0
95109628 9510962 3 C DIPYRONE DIPYRONE 1 0
95109628 9510962 4 C PANTOPRAZOL PANTOPRAZOLE SODIUM 1 0
95109628 9510962 5 C LOSARTAN. LOSARTAN 1 0
95109628 9510962 6 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
95109628 9510962 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
95109628 9510962 OT
95109628 9510962 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
95109628 9510962 Back pain
95109628 9510962 Cholelithiasis
95109628 9510962 Fall
95109628 9510962 Forearm fracture
95109628 9510962 Gamma-glutamyltransferase increased
95109628 9510962 Gastric haemorrhage
95109628 9510962 Hypertension
95109628 9510962 Lower limb fracture
95109628 9510962 Pain
95109628 9510962 Speech disorder
95109628 9510962 Tibia fracture
95109628 9510962 Tracheal injury
95109628 9510962 Traumatic fracture
95109628 9510962 Upper limb fracture

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
95109628 9510962 1 201210 0