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
127019651 12701965 1 I 201608 0 20160830 20160830 DIR 65.00 YR M N 0.00000 20160829 N PH 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
127019651 12701965 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous D D 902723 20170330 0 200 MG QOW
127019651 12701965 3 C CYANOCOBALAM 2 0
127019651 12701965 5 C OMEPRAZOLE. OMEPRAZOLE 1 0
127019651 12701965 7 C METOPROLOL. METOPROLOL 1 0
127019651 12701965 9 C XARELTO RIVAROXABAN 1 0
127019651 12701965 11 C IBUPROFEN. IBUPROFEN 1 0
127019651 12701965 13 C HYDROCO/APAP ACETAMINOPHENHYDROCODONE 1 0
127019651 12701965 15 C LISINOPRIL. LISINOPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127019651 12701965 1 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127019651 12701965 Drug dose omission
127019651 12701965 Fatigue
127019651 12701965 Pain

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

Event ID CASEID RPSR COD
127019651 12701965 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127019651 12701965 1 20141205 0