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
116911806 11691180 6 F 20151023 20160916 20151102 20160920 EXP US-GLAXOSMITHKLINE-US2015152988 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160920 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
116911806 11691180 1 PS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 1 PUFF(S), PRN 5ZP1951 20983 1 DF
116911806 11691180 2 C NORVASC AMLODIPINE BESYLATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116911806 11691180 1 Asthma
116911806 11691180 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
116911806 11691180 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116911806 11691180 Asthma
116911806 11691180 Device use error
116911806 11691180 Drug ineffective
116911806 11691180 Dyspnoea
116911806 11691180 Haemoptysis
116911806 11691180 Nasopharyngitis
116911806 11691180 Pneumonia
116911806 11691180 Product quality issue
116911806 11691180 Pulmonary pain
116911806 11691180 Respiratory tract oedema
116911806 11691180 Secretion discharge
116911806 11691180 Upper respiratory tract infection
116911806 11691180 Wheezing

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
116911806 11691180 1 2005 0