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
1204581626 12045816 26 F 20160119 20160721 20160208 20160722 EXP CA-ROCHE-1707409 ROCHE 64.22 YR F Y 0.00000 20160722 OT 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
1204581626 12045816 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B2048,B2058,B2060,B2050,B2052,B2061 125276 600 MG SOLUTION FOR INFUSION
1204581626 12045816 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B2048,B2058,B2060,B2050,B2052,B2061 125276 300 MG SOLUTION FOR INFUSION
1204581626 12045816 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B2048,B2058,B2060,B2050,B2052,B2061 125276 600 MG SOLUTION FOR INFUSION
1204581626 12045816 4 SS PREDNISONE. PREDNISONE 1 Unknown U 0
1204581626 12045816 5 C TYLENOL ARTHRITIS PAIN ACETAMINOPHEN 1 0
1204581626 12045816 6 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
1204581626 12045816 7 C ATORVASTATIN ATORVASTATIN 1 0
1204581626 12045816 8 C SIMPONI GOLIMUMAB 1 0
1204581626 12045816 9 C BETADERM (CANADA) 2 0
1204581626 12045816 10 C CORTISONE CORTISONEHYDROCORTISONE 1 0
1204581626 12045816 11 C CEFADROXIL. CEFADROXIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1204581626 12045816 1 Rheumatoid arthritis
1204581626 12045816 4 Product used for unknown indication
1204581626 12045816 5 Arthritis

Outcome of event

Event ID CASEID OUTC COD
1204581626 12045816 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1204581626 12045816 Abdominal pain lower
1204581626 12045816 Acne
1204581626 12045816 Arthralgia
1204581626 12045816 Cataract
1204581626 12045816 Chest pain
1204581626 12045816 Dermatitis contact
1204581626 12045816 Diarrhoea
1204581626 12045816 Drug ineffective
1204581626 12045816 Dry skin
1204581626 12045816 Erythema
1204581626 12045816 Fatigue
1204581626 12045816 Haemorrhoids
1204581626 12045816 Joint effusion
1204581626 12045816 Laceration
1204581626 12045816 Madarosis
1204581626 12045816 Malaise
1204581626 12045816 Myalgia
1204581626 12045816 Nocturia
1204581626 12045816 Oropharyngeal pain
1204581626 12045816 Oxygen saturation decreased
1204581626 12045816 Pain
1204581626 12045816 Pain in extremity
1204581626 12045816 Peripheral swelling
1204581626 12045816 Plantar erythema
1204581626 12045816 Pruritus
1204581626 12045816 Pyrexia
1204581626 12045816 Rash erythematous
1204581626 12045816 Sinusitis
1204581626 12045816 Skin atrophy
1204581626 12045816 Skin exfoliation
1204581626 12045816 Vaginal infection
1204581626 12045816 Vulvovaginal mycotic infection

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
1204581626 12045816 1 20160119 0
1204581626 12045816 2 20160401 0
1204581626 12045816 3 20160428 20160630 0