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
92662036 9266203 6 F 20160701 20130502 20160707 EXP BR-ROCHE-1219730 ROCHE 0.00 M Y 68.00000 KG 20160707 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
92662036 9266203 1 PS ACTEMRA TOCILIZUMAB 1 Unknown MOST RECENT DOSE ON 13/MAR/2013 U 125276 INFUSION
92662036 9266203 2 C NATRILIX INDAPAMIDE 1 Unknown 0
92662036 9266203 3 C ENALAPRIL MALEATE. ENALAPRIL MALEATE 1 Unknown 0
92662036 9266203 4 C SELOZOK METOPROLOL SUCCINATE 1 Unknown 0
92662036 9266203 5 C GABAPENTIN. GABAPENTIN 1 Unknown 0
92662036 9266203 6 C ACETYLSALICYLIC ACID ASPIRIN 1 0
92662036 9266203 7 C ENALAPRIL ENALAPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92662036 9266203 1 Rheumatoid arthritis
92662036 9266203 2 Hypertension
92662036 9266203 3 Hypertension
92662036 9266203 4 Hypertension
92662036 9266203 5 Rheumatoid arthritis
92662036 9266203 6 Anticoagulant therapy

Outcome of event

Event ID CASEID OUTC COD
92662036 9266203 HO
92662036 9266203 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
92662036 9266203 Arthropathy
92662036 9266203 Cholelithiasis
92662036 9266203 Depression
92662036 9266203 Erysipelas
92662036 9266203 Hypersensitivity
92662036 9266203 Influenza
92662036 9266203 Lung disorder
92662036 9266203 Lung infection
92662036 9266203 Rheumatoid arthritis

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
92662036 9266203 1 20110511 0