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
127572632 12757263 2 F 201601 20160906 20160919 20160919 EXP GB-CIPLA LTD.-2016GB18137 CIPLA 0.00 Y 0.00000 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
127572632 12757263 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown PRESCRIBED 5MG THEN INCREASED TO 10MG. BUT I REDUCED DOWN TO 5MG AND THEN STOPPED COMPLETELY. Y U 77955

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127572632 12757263 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127572632 12757263 Back pain
127572632 12757263 Constipation
127572632 12757263 Erectile dysfunction
127572632 12757263 Erythema
127572632 12757263 Gingival bleeding
127572632 12757263 Gingival pain
127572632 12757263 Nasal congestion
127572632 12757263 Nasopharyngitis
127572632 12757263 Oedema peripheral
127572632 12757263 Oropharyngeal pain
127572632 12757263 Pain
127572632 12757263 Paraesthesia
127572632 12757263 Productive cough
127572632 12757263 Pruritus
127572632 12757263 Rhinorrhoea
127572632 12757263 Scab
127572632 12757263 Secretion discharge
127572632 12757263 Sinus pain
127572632 12757263 Skin ulcer
127572632 12757263 Somnolence
127572632 12757263 Sputum discoloured
127572632 12757263 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
127572632 12757263 1 201601 201603 0