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
125981342 12598134 2 F 20150224 20160719 20160726 20160729 EXP CA-PFIZER INC-2015073765 PFIZER 59.00 YR F Y 0.00000 20160729 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
125981342 12598134 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 25 MG, WEEKLY N 11719 25 MG SOLUTION FOR INJECTION /wk
125981342 12598134 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 50 MG, UNK N 11719 50 MG SOLUTION FOR INJECTION
125981342 12598134 3 SS ENBREL ETANERCEPT 1 50 MG, WEEKLY N 0 50 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
125981342 12598134 4 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
125981342 12598134 5 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK N 0
125981342 12598134 6 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) UNK U 0
125981342 12598134 7 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 5 MG, BID U 0 5 MG BID
125981342 12598134 8 SS ASA ASPIRIN 1 U 0
125981342 12598134 9 C ACTONEL RISEDRONATE SODIUM 1 35 MG, WEEKLY ON TUESDAY 0 35 MG /wk
125981342 12598134 10 C CALCITE D CALCIUM CARBONATE 1 1500 MG, DAILY (500MG + 1000MG DIE) 0 1500 MG
125981342 12598134 11 C LIPITOR ATORVASTATIN CALCIUM 1 0
125981342 12598134 12 C PANTOLOC PANTOPRAZOLE SODIUM 1 0
125981342 12598134 13 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
125981342 12598134 14 C TYLENOL ACETAMINOPHEN 1 650 MG, 2X/DAY 0 650 MG BID
125981342 12598134 15 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 0
125981342 12598134 16 C DOMPERIDONE DOMPERIDONE 1 0
125981342 12598134 17 C FOLIC ACID. FOLIC ACID 1 5 MG, 6/7 0 5 MG
125981342 12598134 18 C GABAPENTIN. GABAPENTIN 1 0
125981342 12598134 19 C GLICLAZIDE GLICLAZIDE 1 0
125981342 12598134 20 C NIFEDIPINE. NIFEDIPINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125981342 12598134 1 Rheumatoid arthritis
125981342 12598134 3 Rheumatoid arthritis
125981342 12598134 4 Rheumatoid arthritis
125981342 12598134 5 Rheumatoid arthritis
125981342 12598134 6 Rheumatoid arthritis
125981342 12598134 7 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125981342 12598134 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125981342 12598134 Arthralgia
125981342 12598134 Asthenia
125981342 12598134 Back pain
125981342 12598134 Bursitis
125981342 12598134 C-reactive protein abnormal
125981342 12598134 Drug ineffective
125981342 12598134 Drug intolerance
125981342 12598134 Dry mouth
125981342 12598134 Joint range of motion decreased
125981342 12598134 Lip dry
125981342 12598134 Liver disorder
125981342 12598134 Local swelling
125981342 12598134 Lung disorder
125981342 12598134 Muscle spasms
125981342 12598134 Musculoskeletal pain
125981342 12598134 Musculoskeletal stiffness
125981342 12598134 Night sweats
125981342 12598134 Obesity
125981342 12598134 Oedema
125981342 12598134 Oedema peripheral
125981342 12598134 Osteoarthritis
125981342 12598134 Pain
125981342 12598134 Pain in extremity
125981342 12598134 Paraesthesia
125981342 12598134 Peripheral swelling
125981342 12598134 Peripheral venous disease
125981342 12598134 Red blood cell sedimentation rate abnormal
125981342 12598134 Synovitis

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
125981342 12598134 2 201211 0
125981342 12598134 3 20140529 201409 0
125981342 12598134 4 20150304 0
125981342 12598134 5 201305 2014 0