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
126006483 12600648 3 F 201307 20160830 20160727 20160906 EXP JP-SUCAMPO PHARMACEUTICALS, INC.-SPI201600801 SUCAMPO 70.86 YR M Y 0.00000 20160906 PH JP JP

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
126006483 12600648 1 PS AMITIZA LUBIPROSTONE 1 Oral 24 MCG, QD Y 21908 24 UG CAPSULE QD
126006483 12600648 2 SS Magmitt MAGNESIUM OXIDE 1 Oral UNK 0 ORAL DRUG UNSPECIFIED FORM
126006483 12600648 3 C Cetilo SENNA LEAF 1 Oral UNK 0 TABLET
126006483 12600648 4 C LIPITOR ATORVASTATIN CALCIUM 1 Oral UNK 0 TABLET
126006483 12600648 5 C Laxoberon SODIUM PICOSULFATE 1 Oral UNK 0 ORAL DRUG UNSPECIFIED FORM
126006483 12600648 6 C Unknown UNSPECIFIED INGREDIENT 1 Oral UNK 0 ORAL DRUG UNSPECIFIED FORM
126006483 12600648 7 C Unknown UNSPECIFIED INGREDIENT 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126006483 12600648 1 Constipation
126006483 12600648 2 Constipation
126006483 12600648 3 Constipation
126006483 12600648 4 Hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
126006483 12600648 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126006483 12600648 Inappropriate schedule of drug administration
126006483 12600648 Loss of consciousness

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
126006483 12600648 1 20130723 201307 0
126006483 12600648 2 20130723 20150906 0