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
126268892 12626889 2 F 20160812 20160805 20160824 EXP E2B_00566566 CA-HQ SPECIALTY-CA-2016INT000706 INTERCHEM 53.00 YR F Y 0.00000 20160824 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
126268892 12626889 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral UNK Y 201749
126268892 12626889 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral UNK Y 201749
126268892 12626889 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK Y 201749
126268892 12626889 4 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK Y 201749
126268892 12626889 5 SS ENBREL ETANERCEPT 1 Subcutaneous UNK Y 0
126268892 12626889 6 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown UNK Y 0
126268892 12626889 7 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK Y 0
126268892 12626889 8 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK Y 0
126268892 12626889 9 SS ORENCIA ABATACEPT 1 Unknown UNK Y 0
126268892 12626889 10 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK Y 0
126268892 12626889 11 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK Y 0
126268892 12626889 12 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK Y 0
126268892 12626889 13 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK Y 0
126268892 12626889 14 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK Y 0
126268892 12626889 15 C PREDNISONE. PREDNISONE 1 Unknown UNK U 0
126268892 12626889 16 C ADVIL IBUPROFEN 1 Unknown UNK U 0
126268892 12626889 17 C TYLENOL ACETAMINOPHEN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126268892 12626889 1 Rheumatoid arthritis
126268892 12626889 3 Rheumatoid arthritis
126268892 12626889 5 Rheumatoid arthritis
126268892 12626889 6 Rheumatoid arthritis
126268892 12626889 7 Rheumatoid arthritis
126268892 12626889 8 Rheumatoid arthritis
126268892 12626889 9 Rheumatoid arthritis
126268892 12626889 10 Rheumatoid arthritis
126268892 12626889 11 Rheumatoid arthritis
126268892 12626889 12 Rheumatoid arthritis
126268892 12626889 13 Rheumatoid arthritis
126268892 12626889 14 Rheumatoid arthritis
126268892 12626889 15 Product used for unknown indication
126268892 12626889 16 Product used for unknown indication
126268892 12626889 17 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126268892 12626889 Drug intolerance
126268892 12626889 Fatigue
126268892 12626889 Irritable bowel syndrome
126268892 12626889 Malaise
126268892 12626889 Nausea
126268892 12626889 Stress

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
126268892 12626889 1 200705 200708 0
126268892 12626889 2 201001 0
126268892 12626889 3 200705 200708 0
126268892 12626889 4 201001 0
126268892 12626889 5 200710 200804 0
126268892 12626889 6 201308 201312 0
126268892 12626889 7 200701 0
126268892 12626889 8 200806 200810 0
126268892 12626889 9 200812 200905 0
126268892 12626889 10 201105 201108 0
126268892 12626889 11 201006 201010 0
126268892 12626889 12 200909 200911 0