The Safety Rates Drug Report

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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
127410781 12741078 1 I 20150908 20160914 20160914 PER US-TEVA-592490USA TEVA 0.00 F Y 51.00000 KG 20160914 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
127410781 12741078 1 PS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown 80 MILLIGRAM DAILY; 77056 40 MG TABLET BID
127410781 12741078 2 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 77056
127410781 12741078 3 SS DIPHENHYDRAMINE. DIPHENHYDRAMINE 1 Oral 25 OR 50 MG AT BEDTIME U P93574 80738 QD
127410781 12741078 4 C MONTELUKAST MONTELUKAST SODIUM 1 Oral 10 MILLIGRAM DAILY; 0 10 MG TABLET QD
127410781 12741078 5 C CLARITIN LORATADINE 1 Oral 10 MILLIGRAM DAILY; 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127410781 12741078 1 Gastrooesophageal reflux disease
127410781 12741078 2 Gastrooesophageal reflux disease
127410781 12741078 3 Hypersensitivity
127410781 12741078 4 Hypersensitivity
127410781 12741078 5 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127410781 12741078 Drug effect incomplete
127410781 12741078 Drug ineffective
127410781 12741078 Somnolence

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
127410781 12741078 1 2014 2014 0