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
126193982 12619398 2 F 20160729 20160803 20160816 EXP GB-WATSON-2016-16273 WATSON 0.00 A F Y 0.00000 20160816 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
126193982 12619398 1 PS PREDNISOLONE. PREDNISOLONE 1 Oral 6 DF, DAILY Y 150075 80354 6 DF TABLET QD
126193982 12619398 2 C COCODAMOL ACETAMINOPHENCODEINE PHOSPHATE 1 Oral UNK U 0 EFFERVESCENT TABLET
126193982 12619398 3 C MORPHINE MORPHINE 1 Oral UNK U 0 LIQUID
126193982 12619398 4 C VENTOLIN ALBUTEROL SULFATE 1 Unknown UNK U 0
126193982 12619398 5 C CETIRIZINE CETIRIZINE HYDROCHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126193982 12619398 1 Hypersensitivity
126193982 12619398 2 Fibromyalgia
126193982 12619398 3 Spinal pain
126193982 12619398 4 Asthma
126193982 12619398 5 Antiallergic therapy

Outcome of event

Event ID CASEID OUTC COD
126193982 12619398 HO
126193982 12619398 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126193982 12619398 Chest discomfort
126193982 12619398 Dizziness
126193982 12619398 Dry mouth
126193982 12619398 Dry throat
126193982 12619398 Dysphonia
126193982 12619398 Dyspnoea
126193982 12619398 Head discomfort
126193982 12619398 Hypersensitivity
126193982 12619398 Malaise
126193982 12619398 Pyrexia
126193982 12619398 Renal disorder
126193982 12619398 Renal pain

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

no results found

Therapies reported

no results found