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
124382953 12438295 3 F 201601 20160629 20160606 20160705 EXP US-GLAXOSMITHKLINE-US2016079449 GLAXOSMITHKLINE 4.31 YR M Y 0.00000 20160705 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
124382953 12438295 1 PS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 PUFF(S), PRN JL7C 20983 2 DF
124382953 12438295 2 SS VENTOLIN HFA ALBUTEROL SULFATE 1 20983
124382953 12438295 3 SS ALBUTEROL. ALBUTEROL 1 U 20983
124382953 12438295 4 C QVAR BECLOMETHASONE DIPROPIONATE 1 0
124382953 12438295 5 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124382953 12438295 1 Asthma
124382953 12438295 2 Dyspnoea
124382953 12438295 3 Dyspnoea

Outcome of event

Event ID CASEID OUTC COD
124382953 12438295 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124382953 12438295 Atypical pneumonia
124382953 12438295 Bronchiolitis
124382953 12438295 Cough
124382953 12438295 Device use error
124382953 12438295 Drug administered to patient of inappropriate age
124382953 12438295 Drug dose omission
124382953 12438295 Nasopharyngitis
124382953 12438295 Pneumonia
124382953 12438295 Product quality issue
124382953 12438295 Pyrexia
124382953 12438295 Rash
124382953 12438295 Rash erythematous
124382953 12438295 Viral infection
124382953 12438295 Vomiting

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
124382953 12438295 1 2015 0