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
103839322 10383932 2 F 20140714 20140804 20140814 20160707 EXP GB-MYLAN-2014M1000418 MYLAN 0.00 Y 0.00000 20160707 MD GB GB

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
103839322 10383932 1 PS DOXYCYCLINE. DOXYCYCLINE 1 Oral 100 MG, BID 200 MG Y U 21012A 62337 100 MG BID
103839322 10383932 2 SS DOXYCYCLINE. DOXYCYCLINE 1 200 MG Y U 62337
103839322 10383932 3 C FLUTICASONE FLUTICASONEFLUTICASONE PROPIONATE 1 Respiratory (inhalation) 125 MCG CFC INHALER TWO DOSES, TWICE PER DAY. 147000 UG U 0 250 UG BID
103839322 10383932 4 C TIOTROPIUM BROMIDE TIOTROPIUM BROMIDE 1 Respiratory (inhalation) 108 UG 0 18 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103839322 10383932 2 Upper respiratory tract infection
103839322 10383932 3 Product used for unknown indication
103839322 10383932 4 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
103839322 10383932 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
103839322 10383932 Anxiety
103839322 10383932 Depressed mood
103839322 10383932 Dizziness
103839322 10383932 Headache
103839322 10383932 Nausea
103839322 10383932 Palpitations
103839322 10383932 Pruritus
103839322 10383932 Social avoidant behaviour

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
103839322 10383932 1 20140713 20140715 0
103839322 10383932 3 20130923 0
103839322 10383932 4 20140708 0