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
126350281 12635028 1 I 2008 20160728 20160808 20160808 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-49712BP BOEHRINGER INGELHEIM 0.00 M Y 0.00000 20160808 MD 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
126350281 12635028 1 PS CATAPRES-TTS CLONIDINE 1 Oral 0.3571 MG Y 18891 2.5 MG /wk
126350281 12635028 2 SS CATAPRES-TTS CLONIDINE 1 Oral 0.7143 MG Y 18891 5 MG /wk
126350281 12635028 3 SS CATAPRES-TTS CLONIDINE 1 Unknown 0.3571 MG Y 18891 2.5 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126350281 12635028 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126350281 12635028 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126350281 12635028 Drug ineffective
126350281 12635028 Hypotension
126350281 12635028 Intestinal obstruction
126350281 12635028 Renal ischaemia

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
126350281 12635028 1 2008 0
126350281 12635028 2 2008 2016 0
126350281 12635028 3 201605 0