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
119667222 11966722 2 F 201411 20160601 20160127 20160707 EXP BR-ALEXION PHARMACEUTICALS INC-A201600363 ALEXION 31.00 YR F Y 0.00000 20160707 CN BR BR

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
119667222 11966722 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
119667222 11966722 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
119667222 11966722 3 C PEN-VE-ORAL PENICILLIN V POTASSIUM 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119667222 11966722 1 Haemolytic uraemic syndrome
119667222 11966722 3 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
119667222 11966722 HO
119667222 11966722 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119667222 11966722 Abdominal pain lower
119667222 11966722 Arthralgia
119667222 11966722 Blood cholesterol abnormal
119667222 11966722 Dysentery
119667222 11966722 Headache
119667222 11966722 Hypersomnia
119667222 11966722 Hypertension
119667222 11966722 Influenza
119667222 11966722 Insomnia
119667222 11966722 Irritability
119667222 11966722 Mood swings
119667222 11966722 Muscle spasms
119667222 11966722 Pain in extremity
119667222 11966722 Pregnancy
119667222 11966722 Renal impairment
119667222 11966722 Social anxiety disorder
119667222 11966722 Swelling
119667222 11966722 Urinary 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
119667222 11966722 1 20140331 20140421 0
119667222 11966722 2 20140428 0