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
126769531 12676953 1 I 201510 20151014 20160823 20160823 PER US-TEVA-601857USA TEVA 61.82 YR F Y 0.00000 20160823 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
126769531 12676953 1 PS CLONIDINE. CLONIDINE 1 Unknown .3 MILLIGRAM DAILY; UNKNOWN 79090 .3 MG TRANSDERMAL PATCH QD
126769531 12676953 2 SS CLONIDINE. CLONIDINE 1 Unknown .2 MILLIGRAM DAILY; UNKNOWN 79090 .2 MG TRANSDERMAL PATCH QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126769531 12676953 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126769531 12676953 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126769531 12676953 Blood pressure increased
126769531 12676953 Drug ineffective

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found