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
990815631 9908156 31 F 20121218 20160704 20140219 20160713 EXP CA-ROCHE-1185940 ROCHE 51.64 YR F Y 70.00000 KG 20160713 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
990815631 9908156 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B2015B111,B2007B281,B2017B122,B2011 125276 585 MG
990815631 9908156 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B2015B111,B2007B281,B2017B122,B2011 125276 560 MG
990815631 9908156 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B2015B111,B2007B281,B2017B122,B2011 125276 360 MG
990815631 9908156 4 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B2015B111,B2007B281,B2017B122,B2011 125276 560 MG
990815631 9908156 5 SS ACTEMRA TOCILIZUMAB 1 Subcutaneous 125472 162 MG /wk
990815631 9908156 6 SS NAPROXEN. NAPROXEN 1 Unknown B2040, B20243 17581
990815631 9908156 7 SS OMEPRAZOLE. OMEPRAZOLE 1 Unknown U 0
990815631 9908156 8 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown U 0
990815631 9908156 9 C IMURAN AZATHIOPRINE 1 0
990815631 9908156 10 C EMTEC-30 2 0
990815631 9908156 11 C TYLENOL ACETAMINOPHEN 1 Unknown 0
990815631 9908156 12 C LUTEIN LUTEIN 1 0
990815631 9908156 13 C VITAMIN C ASCORBIC ACID 1 0
990815631 9908156 14 C BETA CAROTENE 2 0
990815631 9908156 15 C LOSEC OMEPRAZOLE 1 0
990815631 9908156 16 C FOLIC ACID. FOLIC ACID 1 0
990815631 9908156 17 C VITAMIN E .ALPHA.-TOCOPHEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
990815631 9908156 1 Rheumatoid arthritis
990815631 9908156 5 Rheumatoid arthritis
990815631 9908156 6 Product used for unknown indication
990815631 9908156 7 Product used for unknown indication
990815631 9908156 8 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
990815631 9908156 HO
990815631 9908156 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
990815631 9908156 Arthropathy
990815631 9908156 Arthropod bite
990815631 9908156 Blood pressure increased
990815631 9908156 Bruxism
990815631 9908156 Conjunctivitis
990815631 9908156 Cough
990815631 9908156 Dizziness
990815631 9908156 Fatigue
990815631 9908156 Flatulence
990815631 9908156 Headache
990815631 9908156 Heart rate decreased
990815631 9908156 Hernia
990815631 9908156 Herpes zoster
990815631 9908156 Impaired healing
990815631 9908156 Influenza
990815631 9908156 Infusion related reaction
990815631 9908156 Ingrowing nail
990815631 9908156 Injection site reaction
990815631 9908156 Joint swelling
990815631 9908156 Large intestinal obstruction
990815631 9908156 Localised infection
990815631 9908156 Malaise
990815631 9908156 Mouth injury
990815631 9908156 Nasopharyngitis
990815631 9908156 Oropharyngeal pain
990815631 9908156 Pain
990815631 9908156 Stomatitis
990815631 9908156 Tongue injury
990815631 9908156 Upper respiratory tract 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
990815631 9908156 1 20110901 0
990815631 9908156 2 20120730 0
990815631 9908156 3 20150112 0
990815631 9908156 4 20150216 20160229 0
990815631 9908156 5 20160425 0