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
127437841 12743784 1 I 201601 20160906 20160914 20160914 EXP GB-MHRA-ADR 23621698 PHHY2016GB123170 SANDOZ 0.00 M Y 0.00000 20160914 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
127437841 12743784 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown Y 76859

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127437841 12743784 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127437841 12743784 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127437841 12743784 Back pain
127437841 12743784 Constipation
127437841 12743784 Erectile dysfunction
127437841 12743784 Erythema
127437841 12743784 Gingival bleeding
127437841 12743784 Gingival pain
127437841 12743784 Nasal congestion
127437841 12743784 Nasopharyngitis
127437841 12743784 Oedema peripheral
127437841 12743784 Oropharyngeal pain
127437841 12743784 Pain
127437841 12743784 Paraesthesia
127437841 12743784 Productive cough
127437841 12743784 Pruritus
127437841 12743784 Rhinorrhoea
127437841 12743784 Scab
127437841 12743784 Secretion discharge
127437841 12743784 Sinus pain
127437841 12743784 Skin ulcer
127437841 12743784 Somnolence
127437841 12743784 Sputum discoloured
127437841 12743784 Urticaria

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
127437841 12743784 1 201601 201603 0