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
126117991 12611799 1 I 20150101 20150916 20160801 20160801 PER US-PFIZER INC-3024302 PFIZER 60.00 YR M Y 0.00000 20160801 CN US US

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
126117991 12611799 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 U UNK 11719
126117991 12611799 2 SS ETANERCEPT ETANERCEPT 1 Unknown 50 MG, FREQ:1 DAY; INTERVAL:1. U 1054792 0 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
126117991 12611799 3 C BUDESONIDE W/FORMOTEROL FUMARATE BUDESONIDEFORMOTEROL FUMARATE 1 FREQ:1 DAY; INTERVAL:1. UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126117991 12611799 1 Product used for unknown indication
126117991 12611799 2 Rheumatoid arthritis
126117991 12611799 3 Dyspnoea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126117991 12611799 Dizziness
126117991 12611799 Dyspepsia
126117991 12611799 Dyspnoea
126117991 12611799 Fatigue
126117991 12611799 Headache
126117991 12611799 Increased tendency to bruise
126117991 12611799 Injection site pain
126117991 12611799 Joint swelling
126117991 12611799 Laceration
126117991 12611799 Oral disorder
126117991 12611799 Osteoporosis
126117991 12611799 Sinus congestion
126117991 12611799 Skin atrophy
126117991 12611799 Swelling face
126117991 12611799 Toothache

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
126117991 12611799 2 20150625 0