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
125657552 12565755 2 F 20160707 20160718 20160720 EXP GB-CONCORDIA PHARMACEUTICALS INC.-GSH201607-003498 CONCORDIA 0.00 F Y 0.00000 20160720 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
125657552 12565755 1 PS PREDNISOLONE. PREDNISOLONE 1 Oral Y 150075 21959 6 DF SOLUBLE TABLET
125657552 12565755 2 C Co-codamol effervescent 2 0
125657552 12565755 3 C Morphine MORPHINE 1 Oral 0 ORAL LIQUID
125657552 12565755 4 C VENTOLIN ALBUTEROL SULFATE 1 0
125657552 12565755 5 C CETIRIZINE CETIRIZINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125657552 12565755 1 Hypersensitivity
125657552 12565755 2 Fibromyalgia
125657552 12565755 3 Spinal pain
125657552 12565755 4 Asthma

Outcome of event

Event ID CASEID OUTC COD
125657552 12565755 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125657552 12565755 Chest discomfort
125657552 12565755 Dizziness
125657552 12565755 Dry mouth
125657552 12565755 Dry throat
125657552 12565755 Dysphonia
125657552 12565755 Dyspnoea
125657552 12565755 Head discomfort
125657552 12565755 Hypersensitivity
125657552 12565755 Malaise
125657552 12565755 Pyrexia
125657552 12565755 Renal disorder
125657552 12565755 Renal pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found