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
127815761 12781576 1 I 20160125 20160203 20160926 20160926 PER US-ALLERGAN-1648237 ALLERGAN 77.58 YR F Y 0.00000 20160926 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
127815761 12781576 1 PS CARAFATE SUCRALFATE 1 Oral 1 G/ 10 ML, 4 TIMES DAILY AND ONCE AT NIGHT Y 1153302 19183 1 G ORAL SUSPENSION
127815761 12781576 2 SS CARAFATE SUCRALFATE 1 Y 19183 ORAL SUSPENSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127815761 12781576 1 Gastroenteritis viral
127815761 12781576 2 Abdominal pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127815761 12781576 Abdominal pain upper
127815761 12781576 Abnormal sleep-related event
127815761 12781576 Constipation
127815761 12781576 Fatigue
127815761 12781576 Flatulence
127815761 12781576 Intentional product use issue
127815761 12781576 Middle insomnia
127815761 12781576 Nightmare
127815761 12781576 Product use issue
127815761 12781576 Skin odour abnormal

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
127815761 12781576 1 20160125 0