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
127374511 12737451 1 I 2007 20160531 20160913 20160913 PER US-ASTRAZENECA-2016SE59099 ASTRAZENECA 73.00 YR F Y 86.20000 KG 20160913 CN US US

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
127374511 12737451 1 PS PULMICORT RESPULES BUDESONIDE 1 Respiratory (inhalation) AS NEEDED, 1 VIAL, FREQUENCY UNKNOWN 20929 NEBULISER SUSPENSION
127374511 12737451 2 SS PULMICORT RESPULES BUDESONIDE 1 Respiratory (inhalation) TWO PUFFS TWICE A DAY 20929 INHALATION POWDER
127374511 12737451 3 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 20 MG ONLY AS NEEDED 0 TABLET
127374511 12737451 4 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral SOMETIMES SHE TAKES TWO OF THEM 0 TABLET
127374511 12737451 5 C ESTRADIOL TRANSDERMAL SYSTEM ESTRADIOL 1 Cutaneous 0 BIW
127374511 12737451 6 C FUROSEMIDE. FUROSEMIDE 1 Oral 0 20 MG TIW
127374511 12737451 7 C VITAMIN D CHOLECALCIFEROL 1 Oral 0 QD
127374511 12737451 8 C LOSARTAN. LOSARTAN 1 Oral 0 QD
127374511 12737451 9 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0
127374511 12737451 10 C FUROSEMIDE. FUROSEMIDE 1 0
127374511 12737451 11 C ANTIBIOTICS UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127374511 12737451 1 Dyspnoea
127374511 12737451 2 Dyspnoea
127374511 12737451 3 Gastrooesophageal reflux disease
127374511 12737451 4 Gastrooesophageal reflux disease
127374511 12737451 5 Ill-defined disorder
127374511 12737451 6 Swelling
127374511 12737451 7 Ill-defined disorder
127374511 12737451 8 Blood pressure abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127374511 12737451 Acne
127374511 12737451 Asthenia
127374511 12737451 Balance disorder
127374511 12737451 Blood cholesterol increased
127374511 12737451 Blood pressure decreased
127374511 12737451 Body height decreased
127374511 12737451 Bronchitis
127374511 12737451 Dizziness
127374511 12737451 Dyspnoea
127374511 12737451 Eating disorder
127374511 12737451 Fatigue
127374511 12737451 Feeling abnormal
127374511 12737451 Gait disturbance
127374511 12737451 Intentional product misuse
127374511 12737451 Muscle spasms
127374511 12737451 Neuropathy peripheral
127374511 12737451 Off label use
127374511 12737451 Pancreatitis
127374511 12737451 Product use issue
127374511 12737451 Skin atrophy
127374511 12737451 Skin discolouration
127374511 12737451 Somnolence
127374511 12737451 Swelling
127374511 12737451 Vertigo
127374511 12737451 Weight fluctuation

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
127374511 12737451 1 2006 0
127374511 12737451 2 2014 0
127374511 12737451 3 2006 0
127374511 12737451 4 2006 0
127374511 12737451 5 1985 0
127374511 12737451 6 2007 0