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
127034812 12703481 2 F 20160715 20160728 20160831 20160923 PER US-TEVA-680949USA TEVA 62.72 YR F Y 87.62000 KG 20160923 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
127034812 12703481 1 PS PROAIR HFA ALBUTEROL SULFATE 1 U DAC28A 21457 90 UG
127034812 12703481 2 SS PROVENTIL HFA ALBUTEROL SULFATE 1 Unknown 0
127034812 12703481 3 C LISINOPRIL. LISINOPRIL 1 0
127034812 12703481 4 C ESTRADIOL. ESTRADIOL 1 0
127034812 12703481 5 C FUROSEMIDE. FUROSEMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127034812 12703481 1 Bronchospasm
127034812 12703481 3 Supplementation therapy
127034812 12703481 4 Hormone replacement therapy
127034812 12703481 5 Fluid retention

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127034812 12703481 Cough
127034812 12703481 Dysgeusia
127034812 12703481 Hypoaesthesia oral
127034812 12703481 Nasal congestion
127034812 12703481 Product taste 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
127034812 12703481 1 20160715 0
127034812 12703481 2 20160726 0