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
106468462 10646846 2 F 201410 20160817 20141211 20160819 PER US-009507513-1411USA013028 MERCK 32.73 YR M Y 0.00000 20160819 PH 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
106468462 10646846 1 PS PROVENTIL ALBUTEROL 1 Respiratory (inhalation) 1 PUFF AS NEEDED 140159 20503 1 DF INHALATION POWDER
106468462 10646846 2 SS PROVENTIL ALBUTEROL 1 1 PUFF AS NEEDED 20503 1 DF INHALATION POWDER
106468462 10646846 3 C NAPROXEN. NAPROXEN 1 UNK, PRN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106468462 10646846 1 Respiratory disorder
106468462 10646846 2 Asthma
106468462 10646846 3 Back pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
106468462 10646846 Extra dose administered
106468462 10646846 Product quality issue
106468462 10646846 Throat irritation

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
106468462 10646846 1 1996 0
106468462 10646846 2 1996 0