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
92179805 9217980 5 F 201207 20160729 20130408 20160803 EXP BR-ROCHE-1071923 ROCHE 56.47 YR F Y 88.00000 KG 20160804 CN BR BR

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
92179805 9217980 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) 103705 SOLUTION FOR INFUSION
92179805 9217980 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) 103705 SOLUTION FOR INFUSION
92179805 9217980 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 SOLUTION FOR INFUSION /month
92179805 9217980 4 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 720 MG SOLUTION FOR INFUSION
92179805 9217980 5 SS CALCORT DEFLAZACORT 1 Oral U 0 5 MG BID
92179805 9217980 6 SS CALCORT DEFLAZACORT 1 Oral U 0 12 MG
92179805 9217980 7 SS METHOTREXATE. METHOTREXATE 1 Unknown U 0
92179805 9217980 8 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown U 0
92179805 9217980 9 C LANSOPRAZOLE. LANSOPRAZOLE 1 Oral 0 20 MG QD
92179805 9217980 10 C FLOTAC (BRAZIL) 2 Oral 0 70 MG BID
92179805 9217980 11 C PARACETAMOL ACETAMINOPHEN 1 Unknown 3 TABLETS 0 750 MG
92179805 9217980 12 C PRESS PLUS 2 0
92179805 9217980 13 C LANSOPRAZOLE. LANSOPRAZOLE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92179805 9217980 1 Rheumatoid arthritis
92179805 9217980 3 Rheumatoid arthritis
92179805 9217980 5 Rheumatoid arthritis
92179805 9217980 7 Product used for unknown indication
92179805 9217980 8 Product used for unknown indication
92179805 9217980 9 Prophylaxis
92179805 9217980 10 Premedication
92179805 9217980 11 Premedication
92179805 9217980 12 Hypertension

Outcome of event

Event ID CASEID OUTC COD
92179805 9217980 OT
92179805 9217980 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
92179805 9217980 Abscess
92179805 9217980 Allergy to chemicals
92179805 9217980 Blood pressure decreased
92179805 9217980 Blood pressure fluctuation
92179805 9217980 Cellulitis
92179805 9217980 Chills
92179805 9217980 Condition aggravated
92179805 9217980 Device dislocation
92179805 9217980 Erythema
92179805 9217980 Gait disturbance
92179805 9217980 Gastrointestinal disorder
92179805 9217980 Hypersensitivity
92179805 9217980 Infection
92179805 9217980 Joint injury
92179805 9217980 Medical device removal
92179805 9217980 Migraine
92179805 9217980 Nasopharyngitis
92179805 9217980 Pain
92179805 9217980 Skin discolouration
92179805 9217980 Skin disorder
92179805 9217980 Soft tissue haemorrhage
92179805 9217980 Therapeutic response decreased
92179805 9217980 Throat irritation
92179805 9217980 Thyroid disorder

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
92179805 9217980 1 201009 0
92179805 9217980 2 20090901 0
92179805 9217980 3 20130118 0
92179805 9217980 4 20130118 0
92179805 9217980 5 20130626 0