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
104704669 10470466 9 F 201409 20160719 20140923 20160728 EXP US-SA-2014SA106861 AVENTIS 64.00 YR A F Y 0.00000 20160728 CN US US

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
104704669 10470466 1 PS AUBAGIO TERIFLUNOMIDE 1 Oral U 5HX7ASA 202992 14 MG QD
104704669 10470466 2 SS AUBAGIO TERIFLUNOMIDE 1 Oral U 5HX7ASA 202992 14 MG QD
104704669 10470466 3 SS AUBAGIO TERIFLUNOMIDE 1 Oral U 5HX7ASA 202992 14 MG QD
104704669 10470466 4 SS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 Unknown UNK 0 500 MG BID
104704669 10470466 5 C NITROFURANTOIN. NITROFURANTOIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104704669 10470466 1 Multiple sclerosis
104704669 10470466 2 Multiple sclerosis
104704669 10470466 3 Multiple sclerosis
104704669 10470466 4 Urinary tract infection
104704669 10470466 5 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
104704669 10470466 HO
104704669 10470466 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
104704669 10470466 Activities of daily living impaired
104704669 10470466 Asthenia
104704669 10470466 Balance disorder
104704669 10470466 Bladder discomfort
104704669 10470466 Bladder disorder
104704669 10470466 Blood pressure increased
104704669 10470466 Cardiac failure congestive
104704669 10470466 Cardiomyopathy
104704669 10470466 Carotid artery stenosis
104704669 10470466 Chest pain
104704669 10470466 Diastolic dysfunction
104704669 10470466 Discomfort
104704669 10470466 Drug dose omission
104704669 10470466 Dyspepsia
104704669 10470466 Dyspnoea
104704669 10470466 Ejection fraction decreased
104704669 10470466 Fatigue
104704669 10470466 Gait disturbance
104704669 10470466 Haematocrit increased
104704669 10470466 Haemoglobin increased
104704669 10470466 Malaise
104704669 10470466 Myocardial necrosis marker increased
104704669 10470466 Oxygen saturation decreased
104704669 10470466 Pain in extremity
104704669 10470466 Pain in jaw
104704669 10470466 Palpitations
104704669 10470466 Restrictive pulmonary disease
104704669 10470466 Urinary tract infection
104704669 10470466 Vertigo

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
104704669 10470466 1 20140722 20140910 0
104704669 10470466 2 20140917 20150212 0
104704669 10470466 3 20150424 0