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
127079501 12707950 1 I 201608 20160818 20160901 20160901 EXP US-MALLINCKRODT-T201603943 MALLINCKRODT 43.79 YR F Y 0.00000 20160901 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
127079501 12707950 1 PS Repository Corticotropin Injection CORTICOTROPIN 1 Subcutaneous 80 UNITS TWICE WKLY (MON/THUR) UNKNOWN 8372 INJECTION
127079501 12707950 2 SS MOTRIN IBUPROFEN 1 Unknown UNKNOWN DOSE/FREQUENCY Y UNKNOWN 0
127079501 12707950 3 SS VITAMIN C ASCORBIC ACID 1 Unknown UNKNOWN DOSE/FREQUENCY Y UNKNOWN 0
127079501 12707950 4 SS VITAMIN D CHOLECALCIFEROL 1 Unknown UNKNOWN DOSE/FREQUENCY Y UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127079501 12707950 1 Sarcoidosis
127079501 12707950 2 Product used for unknown indication
127079501 12707950 3 Product used for unknown indication
127079501 12707950 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127079501 12707950 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127079501 12707950 Activities of daily living impaired
127079501 12707950 Bone lesion
127079501 12707950 Inflammation
127079501 12707950 Pain
127079501 12707950 Renal impairment
127079501 12707950 Vertebral lesion

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
127079501 12707950 1 20160331 20160804 0
127079501 12707950 2 2016 0
127079501 12707950 3 2016 0
127079501 12707950 4 2016 0