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
125702121 12570212 1 I 2015 20150728 20160719 20160719 PER US-MALLINCKRODT-T201503689 MALLINCKRODT 0.00 F Y 54.00000 KG 20160719 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
125702121 12570212 1 PS Morphine MORPHINE 1 Oral 60 MG,TID U U 8315Y93452 76438 EXTENDED RELEASE TABLET
125702121 12570212 2 SS Morphine MORPHINE 1 Oral 60 MG, BID U U UNKNOWN 76438 EXTENDED RELEASE TABLET
125702121 12570212 3 SS Morphine MORPHINE 1 Oral 30 MG, TID U U UNKNOWN 76438 EXTENDED RELEASE TABLET
125702121 12570212 4 SS Morphine MORPHINE 1 Oral 30 MG, BID U U UNKNOWN 76438 EXTENDED RELEASE TABLET
125702121 12570212 5 SS Morphine MORPHINE 1 Oral 15 MG QAM AND 30 MG QPM U U UNKNOWN 76438 EXTENDED RELEASE TABLET
125702121 12570212 6 SS Morphine MORPHINE 1 Oral 15 MG, BID U U UNKNOWN 76438 EXTENDED RELEASE TABLET
125702121 12570212 7 SS Morphine MORPHINE 1 Oral 15 MG, QD U U UNKNOWN 76438 EXTENDED RELEASE TABLET
125702121 12570212 8 SS PREDNISONE. PREDNISONE 1 U 0
125702121 12570212 9 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 U 0
125702121 12570212 10 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 U 0
125702121 12570212 11 C CLONAZEPAM. CLONAZEPAM 1 1 MG U 0
125702121 12570212 12 C NORTRIPTYLINE NORTRIPTYLINE 1 10 MG U 0
125702121 12570212 13 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 U 0
125702121 12570212 14 C VITAMIN B12 CYANOCOBALAMIN 1 U 0
125702121 12570212 15 C CALCIUM CALCIUM 1 1200 MG U 0
125702121 12570212 16 C VITAMIN D CHOLECALCIFEROL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125702121 12570212 1 Complex regional pain syndrome

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125702121 12570212 Constipation
125702121 12570212 Drug diversion
125702121 12570212 Drug ineffective
125702121 12570212 Insomnia
125702121 12570212 Micturition urgency
125702121 12570212 Migraine
125702121 12570212 Night sweats

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
125702121 12570212 2 201505 0
125702121 12570212 7 20150725 0