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
126690831 12669083 1 I 20160804 20160819 20160819 EXP US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-121341 RANBAXY 59.00 YR M Y 0.00000 20160819 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
126690831 12669083 1 PS PREDNISONE. PREDNISONE 1 Unknown UNK N UNK 89247
126690831 12669083 2 SS CYCLOSPORINE. CYCLOSPORINE 1 Unknown UNK N U UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126690831 12669083 1 Focal segmental glomerulosclerosis
126690831 12669083 2 Focal segmental glomerulosclerosis

Outcome of event

Event ID CASEID OUTC COD
126690831 12669083 DE
126690831 12669083 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126690831 12669083 Cellulitis
126690831 12669083 Cryptococcal cutaneous infection
126690831 12669083 Disseminated cryptococcosis
126690831 12669083 Pulmonary embolism
126690831 12669083 Sepsis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found