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
124819032 12481903 2 F 201604 20160616 20160620 20160815 PER US-ASTRAZENECA-2016SE53962 ASTRAZENECA 826.00 MON F Y 113.40000 KG 20160815 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
124819032 12481903 1 PS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 21949 180 UG INHALATION POWDER BID
124819032 12481903 2 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) PAKF 21949 2 DF INHALATION POWDER BID
124819032 12481903 3 C ALBUTEROL. ALBUTEROL 1 Respiratory (inhalation) AS REQUIRED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124819032 12481903 1 Asthma
124819032 12481903 2 Asthma
124819032 12481903 3 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124819032 12481903 Cough
124819032 12481903 Device malfunction
124819032 12481903 Drug ineffective
124819032 12481903 Dry throat
124819032 12481903 Malaise
124819032 12481903 Retching
124819032 12481903 Sinusitis

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
124819032 12481903 2 201602 0