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
127439471 12743947 1 I 201601 20160906 20160914 20160914 EXP GB-MHRA-ADR 23621698 GB-MYLANLABS-2016M1037737 MYLAN 0.00 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
127439471 12743947 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 PRESCRIBED 5MG, THEN INCREASED TO 10MG, BUT I REDUCED DOWN TO 5MG AND THEN STOPPED COMPLETELY. Y U 76418

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127439471 12743947 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127439471 12743947 Back pain
127439471 12743947 Constipation
127439471 12743947 Erectile dysfunction
127439471 12743947 Erythema
127439471 12743947 Gingival bleeding
127439471 12743947 Gingival pain
127439471 12743947 Nasal congestion
127439471 12743947 Nasopharyngitis
127439471 12743947 Oedema peripheral
127439471 12743947 Oropharyngeal pain
127439471 12743947 Pain
127439471 12743947 Paraesthesia
127439471 12743947 Productive cough
127439471 12743947 Pruritus
127439471 12743947 Rhinorrhoea
127439471 12743947 Scab
127439471 12743947 Secretion discharge
127439471 12743947 Sinus pain
127439471 12743947 Skin ulcer
127439471 12743947 Somnolence
127439471 12743947 Sputum discoloured
127439471 12743947 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
127439471 12743947 1 201601 201603 0