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
125982491 12598249 1 I 20160704 20160711 20160726 20160726 EXP US-TEVA-676907USA TEVA 87.00 YR F Y 52.21000 KG 20160727 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
125982491 12598249 1 PS PROAIR HFA ALBUTEROL SULFATE 1 Unknown THREE TIMES DAILY AS NEEDED U DECLINED 21457
125982491 12598249 2 SS PROAIR HFA ALBUTEROL SULFATE 1 U DECLINED 21457
125982491 12598249 3 SS ATROVENT IPRATROPIUM BROMIDE 1 Unknown EVERY FOUR TO SIX HOURS U 0
125982491 12598249 4 C ALBUTEROL. ALBUTEROL 1 0 NEBULISER SOLUTION
125982491 12598249 5 C ALBUTEROL. ALBUTEROL 1 0
125982491 12598249 6 C PREDNISONE. PREDNISONE 1 0
125982491 12598249 7 C PREMARIN ESTROGENS, CONJUGATED 1 0
125982491 12598249 8 C CALTRATE WITH VITAMIN D CALCIUM CARBONATECHOLECALCIFEROL 1 0
125982491 12598249 9 C TUMERIC TURMERIC 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125982491 12598249 1 Asthma
125982491 12598249 2 Chronic obstructive pulmonary disease
125982491 12598249 4 Asthma
125982491 12598249 5 Chronic obstructive pulmonary disease
125982491 12598249 6 Pneumonitis
125982491 12598249 7 Hormone replacement therapy
125982491 12598249 8 Supplementation therapy
125982491 12598249 9 Phytotherapy

Outcome of event

Event ID CASEID OUTC COD
125982491 12598249 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125982491 12598249 Eye haemorrhage
125982491 12598249 Ocular hyperaemia

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

no results found

Therapies reported

no results found