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
1152525413 11525254 13 F 201509 20160822 20150918 20160825 EXP CA-PFIZER INC-2015308388 PFIZER 43.00 YR F Y 0.00000 20160825 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
1152525413 11525254 1 SS ENBREL ETANERCEPT 1 Subcutaneous UNK N 0
1152525413 11525254 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 25 MG, UNK N 11719 25 MG
1152525413 11525254 3 SS SULFASALAZINE. SULFASALAZINE 1 Oral 1 G, 2X/DAY N 7073 1 G BID
1152525413 11525254 4 SS REMICADE INFLIXIMAB 1 UNK N 0 POWDER FOR SOLUTION FOR INJECTION
1152525413 11525254 5 SS ACTEMRA TOCILIZUMAB 1 UNK N 0
1152525413 11525254 6 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) UNK N 0
1152525413 11525254 7 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK N 0
1152525413 11525254 8 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK N 0
1152525413 11525254 9 SS RITUXAN RITUXIMAB 1 UNK N 0
1152525413 11525254 10 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK N 0
1152525413 11525254 11 SS ARAVA LEFLUNOMIDE 1 Oral UNK N 0 TABLET
1152525413 11525254 12 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 400 MG, 1X/DAY N 0 400 MG TABLET QD
1152525413 11525254 13 SS CORTISONE CORTISONEHYDROCORTISONE 1 Oral UNK N 0 ORAL DROPS
1152525413 11525254 14 SS FOLIC ACID. FOLIC ACID 1 UNK 0
1152525413 11525254 15 SS PREDNISONE. PREDNISONE 1 UNK 0
1152525413 11525254 16 SS HYDROXYCHLOROQUINE SULFATE. HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK U 0
1152525413 11525254 17 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Unknown UNK U 0
1152525413 11525254 18 C FOSAMAX ALENDRONATE SODIUM 1 UNK 0 TABLET
1152525413 11525254 19 C REACTINE CETIRIZINE HYDROCHLORIDE 1 UNK 0
1152525413 11525254 20 C XELJANZ TOFACITINIB CITRATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1152525413 11525254 1 Rheumatoid arthritis
1152525413 11525254 2 Rheumatoid arthritis
1152525413 11525254 3 Rheumatoid arthritis
1152525413 11525254 4 Rheumatoid arthritis
1152525413 11525254 5 Rheumatoid arthritis
1152525413 11525254 6 Rheumatoid arthritis
1152525413 11525254 7 Rheumatoid arthritis
1152525413 11525254 8 Rheumatoid arthritis
1152525413 11525254 9 Rheumatoid arthritis
1152525413 11525254 10 Rheumatoid arthritis
1152525413 11525254 11 Rheumatoid arthritis
1152525413 11525254 12 Rheumatoid arthritis
1152525413 11525254 13 Rheumatoid arthritis
1152525413 11525254 14 Rheumatoid arthritis
1152525413 11525254 15 Rheumatoid arthritis
1152525413 11525254 16 Rheumatoid arthritis
1152525413 11525254 17 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
1152525413 11525254 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1152525413 11525254 Abdominal discomfort
1152525413 11525254 Alopecia
1152525413 11525254 Drug ineffective
1152525413 11525254 Drug intolerance
1152525413 11525254 Fatigue
1152525413 11525254 Glossodynia
1152525413 11525254 Hand deformity
1152525413 11525254 Infusion related reaction
1152525413 11525254 Pain
1152525413 11525254 Pemphigus
1152525413 11525254 Rash
1152525413 11525254 Swelling
1152525413 11525254 Systemic lupus erythematosus

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
1152525413 11525254 2 2006 2016 0
1152525413 11525254 3 2006 2007 0
1152525413 11525254 6 201005 201103 0
1152525413 11525254 9 2009 2010 0
1152525413 11525254 12 2006 0