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
105290178 10529017 8 F 201303 20160712 20141020 20160727 EXP CA-SYMPLMED PHARMACEUTICALS-2014SYM00126 SYMPLMED PHARMACEUTICALS 0.00 Y 0.00000 20160727 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
105290178 10529017 1 PS Coversyl PERINDOPRIL 1 Unknown UNK N UNKNOWN 20184 TABLET
105290178 10529017 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 1 DF, EVERY 4 WEEKS U B20192 0
105290178 10529017 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 725.6 MG, EVERY 4 WEEKS U UNKNOWN 0
105290178 10529017 4 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 800 MG, EVERY 4 WEEKS U UNKNOWN 0
105290178 10529017 5 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) UNK U UNKNOWN 0
105290178 10529017 6 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 728 MG, EVERY 4 WEEKS U UNKNOWN 0
105290178 10529017 7 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) UNK U UNKNOWN 0
105290178 10529017 8 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) UNK U UNKNOWN 0
105290178 10529017 9 SS APIXABAN APIXABAN 1 Oral 5 MG, BID U U UNKNOWN 0 5 MG
105290178 10529017 10 SS APO-NADOL NADOLOL 1 Unknown UNK N U UNKNOWN 0 TABLET
105290178 10529017 11 SS APO-NADOL NADOLOL 1 Unknown UNK N U UNKNOWN 0 TABLET
105290178 10529017 12 SS LIPITOR ATORVASTATIN CALCIUM 1 Unknown UNK N U UNKNOWN 0
105290178 10529017 13 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown UNK UNKNOWN 0
105290178 10529017 14 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown UNK UNKNOWN 0
105290178 10529017 15 C TYLENOL ACETAMINOPHEN 1 UNK U UNKNOWN 0
105290178 10529017 16 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 UNK U UNKNOWN 0
105290178 10529017 17 C COLECALCIFEROL CHOLECALCIFEROL 1 UNK U UNKNOWN 0
105290178 10529017 18 C CALCIUM CALCIUM 1 UNK U UNKNOWN 0
105290178 10529017 19 C DELATESTRYL TESTOSTERONE ENANTHATE 1 UNK U UNKNOWN 0
105290178 10529017 20 C ESTRADIOL. ESTRADIOL 1 UNK U UNKNOWN 0
105290178 10529017 21 C COZAAR LOSARTAN POTASSIUM 1 UNK U UNKNOWN 0 TABLET
105290178 10529017 22 C FUROSEMIDE. FUROSEMIDE 1 UNK U UNKNOWN 0
105290178 10529017 23 C VITAMIN K NOS 2 UNK U UNKNOWN 0
105290178 10529017 24 C XANAX ALPRAZOLAM 1 UNK U UNKNOWN 0
105290178 10529017 25 C ZOCOR SIMVASTATIN 1 UNK U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105290178 10529017 1 Product used for unknown indication
105290178 10529017 2 Rheumatoid arthritis
105290178 10529017 9 Anticoagulant therapy
105290178 10529017 10 Product used for unknown indication
105290178 10529017 12 Product used for unknown indication
105290178 10529017 13 Product used for unknown indication
105290178 10529017 15 Product used for unknown indication
105290178 10529017 16 Product used for unknown indication
105290178 10529017 17 Product used for unknown indication
105290178 10529017 18 Product used for unknown indication
105290178 10529017 19 Product used for unknown indication
105290178 10529017 20 Product used for unknown indication
105290178 10529017 21 Product used for unknown indication
105290178 10529017 22 Product used for unknown indication
105290178 10529017 23 Product used for unknown indication
105290178 10529017 24 Product used for unknown indication
105290178 10529017 25 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
105290178 10529017 OT
105290178 10529017 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
105290178 10529017 Abasia
105290178 10529017 Abdominal pain
105290178 10529017 Aphthous ulcer
105290178 10529017 Arthralgia
105290178 10529017 Asthenia
105290178 10529017 Atrial fibrillation
105290178 10529017 Bacterial infection
105290178 10529017 Blood pressure increased
105290178 10529017 Bronchitis
105290178 10529017 Bursitis
105290178 10529017 Cardiac failure congestive
105290178 10529017 Chest pain
105290178 10529017 Contusion
105290178 10529017 Cough
105290178 10529017 Deep vein thrombosis
105290178 10529017 Diarrhoea
105290178 10529017 Dysphonia
105290178 10529017 Dyspnoea
105290178 10529017 Ear congestion
105290178 10529017 Epistaxis
105290178 10529017 Fatigue
105290178 10529017 Fungal infection
105290178 10529017 Gait disturbance
105290178 10529017 Headache
105290178 10529017 Heart rate decreased
105290178 10529017 Heart rate irregular
105290178 10529017 Inflammation
105290178 10529017 Infusion related reaction
105290178 10529017 Ligament sprain
105290178 10529017 Migraine
105290178 10529017 Movement disorder
105290178 10529017 Musculoskeletal chest pain
105290178 10529017 Musculoskeletal pain
105290178 10529017 Myalgia
105290178 10529017 Nasal congestion
105290178 10529017 Nasopharyngitis
105290178 10529017 Oral herpes
105290178 10529017 Pain
105290178 10529017 Pain in extremity
105290178 10529017 Peripheral swelling
105290178 10529017 Rash
105290178 10529017 Rectal haemorrhage
105290178 10529017 Sciatica
105290178 10529017 Sinusitis
105290178 10529017 Stress
105290178 10529017 Swelling
105290178 10529017 Thyroid disorder
105290178 10529017 Urinary tract infection
105290178 10529017 Weight decreased
105290178 10529017 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
105290178 10529017 1 2013 20130517 0
105290178 10529017 2 20100721 0
105290178 10529017 10 2013 0
105290178 10529017 11 20130517 0
105290178 10529017 12 2013 20130517 0