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
126175381 12617538 1 I 20160622 20160721 20160803 20160803 EXP GB-MHRA-EYC 00142588 GB-DRREDDYS-GER/UKI/16/0081775 DR REDDYS 37.00 YR M Y 92.07000 KG 20160803 CN 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
126175381 12617538 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral Y U UNKNOWN 76502 180 MG TABLET
126175381 12617538 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral Y U UNKNOWN 76502 180 MG TABLET
126175381 12617538 3 C DYMISTA AZELASTINE HYDROCHLORIDEFLUTICASONE PROPIONATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126175381 12617538 1 Seasonal allergy
126175381 12617538 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126175381 12617538 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126175381 12617538 Agitated depression
126175381 12617538 Anxiety
126175381 12617538 Hyperventilation
126175381 12617538 Panic attack
126175381 12617538 Suicidal ideation

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
126175381 12617538 1 201605 0
126175381 12617538 2 20160519 20160711 0