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
125026563 12502656 3 F 20160805 20160628 20160809 EXP AU-ROCHE-1783918 ROCHE 0.00 M Y 80.00000 KG 20160810 MD AU AU

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
125026563 12502656 1 PS ACTEMRA TOCILIZUMAB 1 Unknown U 125276
125026563 12502656 2 SS PREDNISOLONE. PREDNISOLONE 1 Unknown U 0 9 MG
125026563 12502656 3 C PREDNISONE. PREDNISONE 1 Oral 0 9 MG TABLET QD
125026563 12502656 4 C DICLOFENAC DICLOFENAC 1 Oral 0 50 MG TABLET BID
125026563 12502656 5 C IRBESARTAN. IRBESARTAN 1 Oral 0 75 MG TABLET
125026563 12502656 6 C SIMVASTATIN. SIMVASTATIN 1 Oral 0 10 MG TABLET
125026563 12502656 7 C AMITRIPTYLIN AMITRIPTYLINE 1 Oral 0 10 MG TABLET
125026563 12502656 8 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 20 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125026563 12502656 1 Product used for unknown indication
125026563 12502656 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125026563 12502656 HO
125026563 12502656 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125026563 12502656 Blood electrolytes abnormal
125026563 12502656 Chronic obstructive pulmonary disease
125026563 12502656 Diverticulitis
125026563 12502656 Hypertension
125026563 12502656 Immunodeficiency
125026563 12502656 Intestinal perforation
125026563 12502656 Sepsis

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

no results found

Therapies reported

no results found