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
127576241 12757624 1 I 201601 20160906 20160919 20160919 EXP GB-MHRA-ADR 23621698 GB-ACCORD-043947 ACCORD 0.00 M Y 0.00000 20160919 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
127576241 12757624 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 PRESCRIBED 5MG, THEN INCREASED TO 10MG, BUT PATIENT REDUCED DOWN TO 5MG AND THEN STOPPED COMPLETELY Y 202553

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127576241 12757624 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127576241 12757624 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127576241 12757624 Back pain
127576241 12757624 Constipation
127576241 12757624 Erectile dysfunction
127576241 12757624 Erythema
127576241 12757624 Gingival bleeding
127576241 12757624 Gingival pain
127576241 12757624 Nasal congestion
127576241 12757624 Nasopharyngitis
127576241 12757624 Oedema peripheral
127576241 12757624 Oropharyngeal pain
127576241 12757624 Pain
127576241 12757624 Paraesthesia
127576241 12757624 Productive cough
127576241 12757624 Pruritus
127576241 12757624 Rhinorrhoea
127576241 12757624 Scab
127576241 12757624 Secretion discharge
127576241 12757624 Sinus pain
127576241 12757624 Skin ulcer
127576241 12757624 Somnolence
127576241 12757624 Sputum discoloured
127576241 12757624 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
127576241 12757624 1 201601 201603 0