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
126868211 12686821 1 I 20160818 20160825 20160825 EXP CA-PFIZER INC-2016401507 PFIZER 49.00 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
126868211 12686821 1 SS ENBREL ETANERCEPT 1 Subcutaneous UNK U 0
126868211 12686821 2 PS METHOTREXATE. METHOTREXATE 1 Unknown UNK U 11719
126868211 12686821 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK U 0
126868211 12686821 4 SS PREDNISONE. PREDNISONE 1 Unknown UNK U 0
126868211 12686821 5 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK U 0
126868211 12686821 6 C ACTEMRA TOCILIZUMAB 1 UNK 0
126868211 12686821 7 C CELECOXIB. CELECOXIB 1 UNK 0
126868211 12686821 8 C HYDROMORPHONE HYDROCHLORIDE. HYDROMORPHONE HYDROCHLORIDE 1 Intramuscular UNK 0
126868211 12686821 9 C IBUPROFEN. IBUPROFEN 1 Unknown UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126868211 12686821 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126868211 12686821 Drug ineffective
126868211 12686821 Nausea
126868211 12686821 Respiratory disorder
126868211 12686821 Rheumatoid arthritis
126868211 12686821 Type 2 diabetes mellitus

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

no results found

Therapies reported

no results found