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
117929796 11792979 6 F 20150818 20160919 20151202 20160921 EXP CA-ROCHE-1623648 ROCHE 56.54 YR F Y 88.00000 KG 20160921 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
117929796 11792979 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) ON 01/FEB/2016: LATEST INFUSION B2049,B2033,B2055,B2035,B2062,B2044 125276 640 MG SOLUTION FOR INFUSION
117929796 11792979 2 C TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 0
117929796 11792979 3 C SULPHASALAZINE SULFASALAZINE 1 0
117929796 11792979 4 C LOSEC OMEPRAZOLE 1 0
117929796 11792979 5 C ACTONEL RISEDRONATE SODIUM 1 0
117929796 11792979 6 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 0
117929796 11792979 7 C ASA ASPIRIN 1 0
117929796 11792979 8 C PREDNISONE. PREDNISONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117929796 11792979 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
117929796 11792979 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117929796 11792979 Blood pressure increased
117929796 11792979 Heart rate decreased
117929796 11792979 Hypotension
117929796 11792979 Nasopharyngitis
117929796 11792979 Oral herpes
117929796 11792979 Oxygen saturation decreased
117929796 11792979 Reversible cerebral vasoconstriction syndrome
117929796 11792979 Tooth fracture
117929796 11792979 Weight increased

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
117929796 11792979 1 20150505 0