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
1050318328 10503183 28 F 201409 20160815 20141007 20160817 EXP CA-ROCHE-1446929 ROCHE 64.39 YR F Y 68.00000 KG 20160817 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
1050318328 10503183 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U B20323,B20333,B2040,B2047,B2048,B20 125276 600 MG SOLUTION FOR INFUSION
1050318328 10503183 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral U B2048 0 QD
1050318328 10503183 3 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral U B2048 0 QD
1050318328 10503183 4 SS DILTIAZEM. DILTIAZEM 1 Unknown 0
1050318328 10503183 5 C METHOTREXATE. METHOTREXATE 1 0
1050318328 10503183 6 C FOLIC ACID. FOLIC ACID 1 0
1050318328 10503183 7 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown SINCE 10 YEAR 0
1050318328 10503183 8 C OMEPRAZOL OMEPRAZOLE 1 Unknown 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1050318328 10503183 1 Rheumatoid arthritis
1050318328 10503183 2 Blood cholesterol increased
1050318328 10503183 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1050318328 10503183 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1050318328 10503183 Arthralgia
1050318328 10503183 Asthma
1050318328 10503183 Back pain
1050318328 10503183 Blood cholesterol increased
1050318328 10503183 Blood pressure increased
1050318328 10503183 Body temperature decreased
1050318328 10503183 Bronchitis
1050318328 10503183 Cough
1050318328 10503183 Diarrhoea
1050318328 10503183 Drug effect decreased
1050318328 10503183 Eczema
1050318328 10503183 Fall
1050318328 10503183 Fatigue
1050318328 10503183 Gastrooesophageal reflux disease
1050318328 10503183 Heart rate increased
1050318328 10503183 Hypertension
1050318328 10503183 Hypotension
1050318328 10503183 Infusion related reaction
1050318328 10503183 Joint swelling
1050318328 10503183 Muscle spasms
1050318328 10503183 Muscular weakness
1050318328 10503183 Nasopharyngitis
1050318328 10503183 Oesophageal pain
1050318328 10503183 Oral discomfort
1050318328 10503183 Oropharyngeal pain
1050318328 10503183 Oxygen saturation decreased
1050318328 10503183 Pain
1050318328 10503183 Pain in extremity
1050318328 10503183 Peripheral swelling
1050318328 10503183 Precancerous cells present
1050318328 10503183 Seasonal allergy
1050318328 10503183 Sinusitis
1050318328 10503183 Skin swelling
1050318328 10503183 Swelling
1050318328 10503183 Vertigo
1050318328 10503183 Weight decreased
1050318328 10503183 Weight increased

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
1050318328 10503183 1 20140805 0