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
125959883 12595988 3 F 2016 20160830 20160727 20160902 EXP IE-ALEXION PHARMACEUTICALS INC-A201604735 ALEXION 56.54 YR F Y 0.00000 20160902 PH IE IE

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
125959883 12595988 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W P0004202 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
125959883 12595988 2 C FOLIC ACID. FOLIC ACID 1 Unknown 0 TABLET
125959883 12595988 3 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Unknown 0 TABLET
125959883 12595988 4 C SALBUTAMOL ALBUTEROL 1 Other UNK, INHALER 0 INHALATION GAS
125959883 12595988 5 C VENTOLIN ALBUTEROL SULFATE 1 Other 5 MG, QDS 0 5 MG
125959883 12595988 6 C TAVANIC LEVOFLOXACIN 1 Other 250 MG, QD 0 250 MG QD
125959883 12595988 7 C PARACETAMOL ACETAMINOPHEN 1 Other 500 MG, PRN 0 500 MG /yr
125959883 12595988 8 C CLOROM CLARITHROMYCIN 1 Unknown UNK, QD 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125959883 12595988 1 Paroxysmal nocturnal haemoglobinuria
125959883 12595988 2 Product used for unknown indication
125959883 12595988 3 Product used for unknown indication
125959883 12595988 4 Product used for unknown indication
125959883 12595988 5 Product used for unknown indication
125959883 12595988 6 Product used for unknown indication
125959883 12595988 7 Product used for unknown indication
125959883 12595988 8 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125959883 12595988 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125959883 12595988 Arthralgia
125959883 12595988 Bone pain
125959883 12595988 Haemoglobin decreased
125959883 12595988 Infusion related reaction
125959883 12595988 Pain in extremity
125959883 12595988 Pelvic pain

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
125959883 12595988 1 20101229 0