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
125184102 12518410 2 F 20160407 20160725 20160630 20160728 EXP GB-002147023-PHFR2016GB002801 GB-GALDERMA-GB16004331 GALDERMA 41.00 YR F Y 0.00000 20160728 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
125184102 12518410 1 PS DOXYCYCLINE. DOXYCYCLINE 1 U 50783
125184102 12518410 2 SS CAPECITABINE. CAPECITABINE 1 0
125184102 12518410 3 SS TYVERB LAPATINIB 1 0
125184102 12518410 4 SS CLEXANE ENOXAPARIN SODIUM 1 Subcutaneous 0 INJECTION
125184102 12518410 5 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 0 INJECTION
125184102 12518410 6 SS LOPERAMIDE LOPERAMIDE 1 0
125184102 12518410 7 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125184102 12518410 1 Acne
125184102 12518410 2 Product used for unknown indication
125184102 12518410 3 Product used for unknown indication
125184102 12518410 4 Product used for unknown indication
125184102 12518410 5 Product used for unknown indication
125184102 12518410 6 Product used for unknown indication
125184102 12518410 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125184102 12518410 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125184102 12518410 Abasia
125184102 12518410 Acne
125184102 12518410 Anxiety
125184102 12518410 Contusion
125184102 12518410 Depression
125184102 12518410 Diarrhoea
125184102 12518410 Dyspnoea
125184102 12518410 Eating disorder
125184102 12518410 Fatigue
125184102 12518410 Gastritis
125184102 12518410 Headache
125184102 12518410 Inflammatory pain
125184102 12518410 Insomnia
125184102 12518410 Intentional product use issue
125184102 12518410 Malaise
125184102 12518410 Muscle spasms
125184102 12518410 Onychalgia
125184102 12518410 Oropharyngeal pain
125184102 12518410 Pain in extremity
125184102 12518410 Peripheral swelling
125184102 12518410 Plantar erythema
125184102 12518410 Pruritus
125184102 12518410 Speech disorder
125184102 12518410 Vomiting

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
125184102 12518410 1 20160324 0