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
127559111 12755911 1 I 20151119 20151202 20160916 20160916 PER US-TELIGENT, INC-IGIL20150036 TELIGENT 57.31 YR F Y 90.30000 KG 20160916 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
127559111 12755911 1 PS RANITIDINE HYDROCHLORIDE. RANITIDINE HYDROCHLORIDE 1 Unknown U 19090 UNKNOWN
127559111 12755911 2 C COMPAZINE PROCHLORPERAZINE MALEATE 1 Unknown 0 UNKNOWN
127559111 12755911 3 C COMPAZINE PROCHLORPERAZINE MALEATE 1 0
127559111 12755911 4 C COMPAZINE PROCHLORPERAZINE MALEATE 1 0
127559111 12755911 5 C BENTYL DICYCLOMINE HYDROCHLORIDE 1 Unknown 0 UNKNOWN
127559111 12755911 6 C TOVIAZ FESOTERODINE FUMARATE 1 Oral 0 UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127559111 12755911 1 Gastrooesophageal reflux disease
127559111 12755911 2 Poor quality sleep
127559111 12755911 3 Nausea
127559111 12755911 4 Abdominal discomfort
127559111 12755911 5 Poor quality sleep
127559111 12755911 6 Hypertonic bladder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127559111 12755911 Drug ineffective

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
127559111 12755911 1 20151119 0
127559111 12755911 2 20151119 0
127559111 12755911 6 20151117 0