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
127419571 12741957 1 I 201601 20160906 20160914 20160914 EXP GB-MHRA-ADR 23621698 GB-TEVA-692437ACC TEVA 0.00 M Y 0.00000 20160914 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
127419571 12741957 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 PRESCRIBED 5MG, THEN INCREASED TO 10MG, BUT I REDUCED DOWN TO 5MG AND THEN STOPPED COMPLETELY. Y U 76846

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127419571 12741957 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127419571 12741957 Back pain
127419571 12741957 Constipation
127419571 12741957 Erectile dysfunction
127419571 12741957 Erythema
127419571 12741957 Gingival bleeding
127419571 12741957 Gingival pain
127419571 12741957 Nasal congestion
127419571 12741957 Nasopharyngitis
127419571 12741957 Oedema peripheral
127419571 12741957 Oropharyngeal pain
127419571 12741957 Pain
127419571 12741957 Paraesthesia
127419571 12741957 Productive cough
127419571 12741957 Pruritus
127419571 12741957 Rhinorrhoea
127419571 12741957 Scab
127419571 12741957 Secretion discharge
127419571 12741957 Sinus pain
127419571 12741957 Skin ulcer
127419571 12741957 Somnolence
127419571 12741957 Sputum discoloured
127419571 12741957 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
127419571 12741957 1 201601 201603 0