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
125745342 12574534 2 F 2015 20160802 20160720 20160808 EXP CA-GLAXOSMITHKLINE-CA2015GSK016839 GLAXOSMITHKLINE 74.09 YR F Y 52.00000 KG 20160808 CN CA CA

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
125745342 12574534 1 SS Volibris AMBRISENTAN 1 Oral 5 MG, QD U 0 5 MG QD
125745342 12574534 2 SS Ampicillin AMPICILLIN 1 UNK U 0 SUPPOSITORY
125745342 12574534 3 PS Salbutamol ALBUTEROL 1 UNK U 20983
125745342 12574534 4 SS NOVO-SALBUTAMOL HFA ALBUTEROL 1 2 PUFF(S), UNK 0 2 DF
125745342 12574534 5 C DICETEL PINAVERIUM BROMIDE 1 UNK U 0
125745342 12574534 6 C SALBUTAMOL ALBUTEROL 1 UNK U 0
125745342 12574534 7 C TECTA PANTOPRAZOLE MAGNESIUM 1 UNK U 0
125745342 12574534 8 C ZOPLICONE ZOPICLONE 1 U 0
125745342 12574534 9 C AMITRIPTYLINE AMITRIPTYLINE 1 U 0
125745342 12574534 10 C APO-MOMETASONE MOMETASONE FUROATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125745342 12574534 1 Pulmonary arterial hypertension
125745342 12574534 2 Dental operation
125745342 12574534 3 Product used for unknown indication
125745342 12574534 4 Product used for unknown indication
125745342 12574534 5 Product used for unknown indication
125745342 12574534 6 Product used for unknown indication
125745342 12574534 7 Product used for unknown indication
125745342 12574534 8 Product used for unknown indication
125745342 12574534 9 Product used for unknown indication
125745342 12574534 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125745342 12574534 HO
125745342 12574534 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125745342 12574534 Abdominal discomfort
125745342 12574534 Abdominal pain upper
125745342 12574534 Asthenia
125745342 12574534 Chest pain
125745342 12574534 Cough
125745342 12574534 Drug interaction
125745342 12574534 Drug intolerance
125745342 12574534 Enamel anomaly
125745342 12574534 Fatigue
125745342 12574534 Gastric antral vascular ectasia
125745342 12574534 Gingival recession
125745342 12574534 Headache
125745342 12574534 Heart rate increased
125745342 12574534 Helminthic infection
125745342 12574534 Influenza
125745342 12574534 Pain
125745342 12574534 Product use issue
125745342 12574534 Rectal haemorrhage
125745342 12574534 Sinus congestion
125745342 12574534 Sleep disorder
125745342 12574534 Tooth disorder
125745342 12574534 Weight 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
125745342 12574534 1 20140510 0
125745342 12574534 2 2015 0