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
127005541 12700554 1 I 20160822 20160830 20160830 EXP CA-PFIZER INC-2016406909 PFIZER 61.00 YR M Y 0.00000 20160830 OT 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
127005541 12700554 1 SS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, QWK U 0 50 MG /wk
127005541 12700554 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 10 MG, QWK U 11719 10 MG TABLET /wk
127005541 12700554 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 25 MG, QWK U 11719 25 MG TABLET /wk
127005541 12700554 4 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 200 MG, UNK U 0 200 MG
127005541 12700554 5 SS VIOXX ROFECOXIB 1 Unknown 12.5 MG, QD U 0 12.5 MG TABLET QD
127005541 12700554 6 C MOBICOX MELOXICAM 1 Oral UNK UNK, QD 0
127005541 12700554 7 C MOTRIN IBUPROFEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127005541 12700554 1 Ankylosing spondylitis

Outcome of event

Event ID CASEID OUTC COD
127005541 12700554 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127005541 12700554 Drug ineffective
127005541 12700554 Hypertension
127005541 12700554 Iritis
127005541 12700554 Nervous system disorder
127005541 12700554 Rheumatoid arthritis

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

no results found

Therapies reported

no results found