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
118352215 11835221 5 F 2010 20160809 20151215 20160823 EXP GB-MHRA-ADR 22272189 GB-ACCORD-036147 ACCORD 71.00 YR F Y 0.00000 20160823 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
118352215 11835221 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown U 202553
118352215 11835221 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous ALSO RECEIVED 600 MG U B1010B08 0 450 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118352215 11835221 1 Product used for unknown indication
118352215 11835221 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118352215 11835221 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118352215 11835221 Arthralgia
118352215 11835221 Bladder irritation
118352215 11835221 Blood pressure increased
118352215 11835221 Dizziness
118352215 11835221 Dry skin
118352215 11835221 Dysuria
118352215 11835221 Fall
118352215 11835221 Fatigue
118352215 11835221 Feeling abnormal
118352215 11835221 Gingival pain
118352215 11835221 Head injury
118352215 11835221 Hepatic neoplasm
118352215 11835221 Joint swelling
118352215 11835221 Lacrimation increased
118352215 11835221 Local swelling
118352215 11835221 Musculoskeletal stiffness
118352215 11835221 Myalgia
118352215 11835221 Nasal congestion
118352215 11835221 Neoplasm progression
118352215 11835221 Onychoclasis
118352215 11835221 Photophobia
118352215 11835221 Pruritus
118352215 11835221 Rhinorrhoea
118352215 11835221 Sinus pain
118352215 11835221 Skin abrasion
118352215 11835221 Tenderness
118352215 11835221 Trigeminal neuralgia
118352215 11835221 Urinary retention
118352215 11835221 Urine flow decreased

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
118352215 11835221 1 201509 0
118352215 11835221 2 2010 0