The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
4959782 6016860 F 4959782-2 20051019 20051108 20060331 EXP US-BOEHRINGER INGELHEIM PHARMACEUTICALS, INC.-2005-BP-19578BP BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. F Y 20060331 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
4959782 1007117958 PS SPIRIVA 1 RESPIRATORY (INHALATION) 405281 021395
4959782 1007117959 SS SPIRIVA 1 RESPIRATORY (INHALATION) 405281 021395
4959782 1007117960 SS SPIRIVA 1 RESPIRATORY (INHALATION) 405281 021395
4959782 1007117961 C THEOPHYLLINE 1 ORAL
4959782 1007117962 C BRETHINE 1
4959782 1007117963 C LORAZEPAM 1
4959782 1007117964 C TERBUTALINE 2
4959782 1007117965 C XOPENEX 1
4959782 1007117966 C PROTONIX 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4959782 1007117958 CHRONIC OBSTRUCTIVE PULMONARY DISEASE

Outcome of event

Event ID OUTC COD
4959782 HO

Reactions reported

Event ID PT
4959782 CHOKING
4959782 COUGH
4959782 DRY MOUTH
4959782 DRY THROAT
4959782 GINGIVAL PAIN
4959782 GLOSSODYNIA
4959782 HAEMOPTYSIS
4959782 ORAL CANDIDIASIS
4959782 TONGUE DISCOLOURATION
4959782 VISION BLURRED
4959782 WEIGHT DECREASED

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4959782 1007117958 20051018 20051104
4959782 1007117959 20051105
4959782 1007117960 20060101 20060301