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
127232241 12723224 1 I 20160805 20160908 20160908 EXP US-ROCHE-1809905 ROCHE 1.00 YR M Y 0.00000 20160908 CN US US

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
127232241 12723224 1 PS ACTEMRA TOCILIZUMAB 1 Subcutaneous U 125472 162 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
127232241 12723224 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 SOLUTION FOR INFUSION
127232241 12723224 3 SS NAPROXEN. NAPROXEN 1 Unknown U 17581
127232241 12723224 4 C METHOTREXATE. METHOTREXATE 1 0
127232241 12723224 5 C PREDNISOLONE. PREDNISOLONE 1 0
127232241 12723224 6 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0
127232241 12723224 7 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127232241 12723224 1 Juvenile idiopathic arthritis
127232241 12723224 2 Juvenile idiopathic arthritis
127232241 12723224 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127232241 12723224 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127232241 12723224 Arthralgia
127232241 12723224 Drug effect decreased
127232241 12723224 Ileus
127232241 12723224 Off label use
127232241 12723224 Pyrexia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found