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
126192081 12619208 1 I 20160720 20160803 20160803 EXP E2B_00523801 CA-HQ SPECIALTY-CA-2016INT000650 INTERCHEM 0.00 F Y 0.00000 20160803 CN 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
126192081 12619208 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U 201749
126192081 12619208 2 SS ENBREL ETANERCEPT 1 Unknown UNK U 0
126192081 12619208 3 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK U 0
126192081 12619208 4 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126192081 12619208 1 Rheumatoid arthritis
126192081 12619208 2 Rheumatoid arthritis
126192081 12619208 3 Rheumatoid arthritis
126192081 12619208 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126192081 12619208 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126192081 12619208 Arthropathy
126192081 12619208 Diarrhoea
126192081 12619208 Drug ineffective
126192081 12619208 Lung disorder
126192081 12619208 Nausea
126192081 12619208 Vomiting

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

no results found

Therapies reported

no results found