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
126122931 12612293 1 I 20160725 20160801 20160801 EXP PHHY2016BR103772 NOVARTIS 0.00 F Y 92.00000 KG 20160801 CN BR BR

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
126122931 12612293 1 SS FORASEQ BUDESONIDEFORMOTEROL FUMARATE 1 Respiratory (inhalation) UNK UNK, BID (EVERY 12 HOURS) 15J27LA 0 CAPSULE BID
126122931 12612293 2 PS DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 Oral 1 DF, QD 20818 1 DF TABLET QD
126122931 12612293 3 C AEROLIN ALBUTEROL 1 Unknown U 0
126122931 12612293 4 C HIDROMED HYDROCHLOROTHIAZIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126122931 12612293 1 Dyspnoea
126122931 12612293 2 Hypertension
126122931 12612293 3 Product used for unknown indication
126122931 12612293 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126122931 12612293 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126122931 12612293 Drug dependence
126122931 12612293 Drug ineffective for unapproved indication
126122931 12612293 Feeling abnormal
126122931 12612293 Increased upper airway secretion
126122931 12612293 Product use issue

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

no results found

Therapies reported

no results found