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
119952326 11995232 6 F 2015 20160905 20160203 20160912 EXP US-SA-2015SA181047 AVENTIS 27.00 YR A F Y 127.01000 KG 20160912 OT 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
119952326 11995232 1 PS LEMTRADA ALEMTUZUMAB 1 Intravenous drip UNKNOWN 103948 12 MG CONCENTRATE FOR SOLUTION FOR INFUSION QD
119952326 11995232 2 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Intravenous (not otherwise specified) U UNKNOWN 0 1000 MG
119952326 11995232 3 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0 50 MG
119952326 11995232 4 C MOTRIN IBUPROFEN 1 Oral 0 600 MG
119952326 11995232 5 C MOTRIN IBUPROFEN 1 Oral 0 600 MG
119952326 11995232 6 C TYLENOL ACETAMINOPHEN 1 0 650 MG
119952326 11995232 7 C IRON IRON 1 0 TID
119952326 11995232 8 C ZANAFLEX TIZANIDINE HYDROCHLORIDE 1 0 TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119952326 11995232 1 Multiple sclerosis
119952326 11995232 2 Premedication
119952326 11995232 3 Premedication
119952326 11995232 4 Premedication
119952326 11995232 5 Pain
119952326 11995232 6 Pain
119952326 11995232 7 Blood count abnormal
119952326 11995232 8 Muscle relaxant therapy

Outcome of event

Event ID CASEID OUTC COD
119952326 11995232 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119952326 11995232 Abdominal pain
119952326 11995232 Anxiety
119952326 11995232 Asthenia
119952326 11995232 Barrett's oesophagus
119952326 11995232 Candida infection
119952326 11995232 Chest discomfort
119952326 11995232 Chest pain
119952326 11995232 Choking sensation
119952326 11995232 Cough
119952326 11995232 Diplopia
119952326 11995232 Dysphagia
119952326 11995232 Dyspnoea
119952326 11995232 Epistaxis
119952326 11995232 Fall
119952326 11995232 Head injury
119952326 11995232 Headache
119952326 11995232 Hypertension
119952326 11995232 Hypoaesthesia
119952326 11995232 Loss of consciousness
119952326 11995232 Maternal exposure before pregnancy
119952326 11995232 Memory impairment
119952326 11995232 Menorrhagia
119952326 11995232 Migraine
119952326 11995232 Nausea
119952326 11995232 Neck pain
119952326 11995232 Oropharyngeal pain
119952326 11995232 Pain
119952326 11995232 Pruritus
119952326 11995232 Scar
119952326 11995232 Vomiting
119952326 11995232 White blood cell count increased
119952326 11995232 Wound

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
119952326 11995232 1 20151102 20151106 0
119952326 11995232 2 20151102 20151106 0
119952326 11995232 3 20151102 20151106 0
119952326 11995232 4 20151102 20151106 0
119952326 11995232 5 20151102 20151106 0
119952326 11995232 6 20151103 20151104 0