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
127364141 12736414 1 I 201601 20160906 20160913 20160913 EXP GB-MHRA-ADR 23621698 GB-DRREDDYS-GER/UKI/16/0083059 DR REDDYS 0.00 M Y 0.00000 20160913 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
127364141 12736414 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 PRESCRIBED 5MG, THEN INCREASED TO 10MG, BUT I REDUCED DOWN TO 5MG AND THEN STOPPED COMPLETELY. Y U UNKNOWN 76692

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127364141 12736414 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127364141 12736414 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127364141 12736414 Back pain
127364141 12736414 Constipation
127364141 12736414 Erectile dysfunction
127364141 12736414 Erythema
127364141 12736414 Gingival bleeding
127364141 12736414 Gingival pain
127364141 12736414 Nasal congestion
127364141 12736414 Nasopharyngitis
127364141 12736414 Oedema peripheral
127364141 12736414 Oropharyngeal pain
127364141 12736414 Pain
127364141 12736414 Paraesthesia
127364141 12736414 Productive cough
127364141 12736414 Pruritus
127364141 12736414 Rhinorrhoea
127364141 12736414 Scab
127364141 12736414 Secretion discharge
127364141 12736414 Sinus pain
127364141 12736414 Skin ulcer
127364141 12736414 Somnolence
127364141 12736414 Sputum discoloured
127364141 12736414 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
127364141 12736414 1 201601 201603 0