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
124925192 12492519 2 F 20160623 20160623 20160701 EXP US-009507513-1606USA007369 MERCK 0.00 F Y 0.00000 20160701 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
124925192 12492519 1 PS ALBUTEROL SULFATE. ALBUTEROL SULFATE 1 UNK U 20503 INHALATION POWDER
124925192 12492519 2 SS FORADIL FORMOTEROL FUMARATE 1 UNK U 0
124925192 12492519 3 SS PERFOROMIST FORMOTEROL FUMARATE DIHYDRATE 1 UNK 0
124925192 12492519 4 C ASMANEX MOMETASONE FUROATE 1 UNK U 0 INHALATION POWDER
124925192 12492519 5 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
124925192 12492519 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124925192 12492519 Abdominal discomfort
124925192 12492519 Anxiety
124925192 12492519 Dizziness
124925192 12492519 Drug hypersensitivity
124925192 12492519 Extra dose administered
124925192 12492519 Feeling abnormal
124925192 12492519 Heart rate increased
124925192 12492519 Hypopnoea
124925192 12492519 Muscle spasms
124925192 12492519 Product taste abnormal
124925192 12492519 Pruritus
124925192 12492519 Pulmonary fibrosis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found