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
98298163 9829816 3 F 20140109 20140123 20140120 20151001 EXP US-ROCHE-1334501 ROCHE 59.08 YR F Y 63.56000 KG 20151001 MD 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
98298163 9829816 1 PS ACTEMRA TOCILIZUMAB 1 Subcutaneous 81002802 125472 162 MG QOW
98298163 9829816 2 SS ACTEMRA TOCILIZUMAB 1 Subcutaneous 81002802 125472 162 MG
98298163 9829816 3 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 0
98298163 9829816 4 C GRALISE GABAPENTIN 1 Unknown 0 1800 MG QD
98298163 9829816 5 C FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 0
98298163 9829816 6 C AMBIEN ZOLPIDEM TARTRATE 1 Unknown PRN 0
98298163 9829816 7 C TYLENOL ACETAMINOPHEN 1 0
98298163 9829816 8 C PREDNISONE. PREDNISONE 1 Unknown 0 7.5 MG QD
98298163 9829816 9 C FOLIC ACID. FOLIC ACID 1 Unknown 0 1 MG QD
98298163 9829816 10 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98298163 9829816 1 Rheumatoid arthritis
98298163 9829816 8 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
98298163 9829816 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98298163 9829816 Blood urine present
98298163 9829816 Dysuria
98298163 9829816 Headache
98298163 9829816 Skin exfoliation
98298163 9829816 Urethral haemorrhage

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
98298163 9829816 1 20131230 0
98298163 9829816 2 20140113 0