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
126337252 12633725 2 F 20160729 20160915 20160809 20160919 EXP GB-MHRA-TPP30711593C2823597YC1469779792196 GB-GALDERMA-GB16005407 GALDERMA 57.00 YR F Y 46.00000 KG 20160919 OT 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
126337252 12633725 1 PS DOXYCYCLINE. DOXYCYCLINE 1 U 50783
126337252 12633725 2 C CALCIPOTRIOL CALCIPOTRIENE 1 0 1 DF BID
126337252 12633725 3 C LEFLUNOMIDE. LEFLUNOMIDE 1 0 20 MG QD
126337252 12633725 4 C CALCIUM CARBONATE. CALCIUM CARBONATE 1 0 1 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126337252 12633725 1 Lower respiratory tract infection
126337252 12633725 2 Product used for unknown indication
126337252 12633725 3 Product used for unknown indication
126337252 12633725 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126337252 12633725 LT
126337252 12633725 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126337252 12633725 Anaphylactic reaction
126337252 12633725 Loss of consciousness
126337252 12633725 Nausea
126337252 12633725 Rash

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
126337252 12633725 1 20160729 0
126337252 12633725 2 20160229 0
126337252 12633725 3 20160229 0
126337252 12633725 4 20160229 0