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
123766162 12376616 2 F 20150520 20160517 20160517 PER US-MALLINCKRODT-T201502691 MALLINCKRODT 0.00 M Y 0.00000 20160517 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
123766162 12376616 1 PS Repository Corticotropin Injection CORTICOTROPIN 1 Subcutaneous 80 UNITS TWICE WKLY UNKNOWN 8372 INJECTION
123766162 12376616 2 SS CYCLOSPORINE. CYCLOSPORINE 1 Unknown U UNKNOWN 0
123766162 12376616 3 I FUROSEMIDE. FUROSEMIDE 1 Unknown UNK U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123766162 12376616 1 Nephrotic syndrome
123766162 12376616 2 Product used for unknown indication
123766162 12376616 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123766162 12376616 Diarrhoea
123766162 12376616 Dysgeusia
123766162 12376616 Fatigue
123766162 12376616 Labelled drug-drug interaction medication error
123766162 12376616 Muscle spasms
123766162 12376616 Parosmia
123766162 12376616 Protein total increased
123766162 12376616 Purpura
123766162 12376616 Swelling

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
123766162 12376616 1 20150113 0