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
4960036 6010844 F 4960036-9 19990916 20050901 20060331 EXP US-MERCK-0509USA00506 MERCK HUMAN HEALTH DIVISION 83 YR F Y 71 KG 20060403 LW 20010307 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
4960036 1007118995 PS VIOXX 1 ORAL 21042
4960036 1007118996 SS VIOXX 1 ORAL 021042
4960036 1007118997 SS VIOXX 1 ORAL 021042
4960036 1007118998 SS VIOXX 1 ORAL 021042
4960036 1007118999 C COVERA-HS 1 ORAL
4960036 1007119000 C PEPCID 1 ORAL
4960036 1007119001 C FLONASE 1 UNKNOWN
4960036 1007119002 C TOPROL-XL 1 ORAL
4960036 1007119003 C LEVAQUIN 1 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
4960036 1007118995 OSTEOARTHRITIS
4960036 1007118997 BACK PAIN
4960036 1007118999 SUPRAVENTRICULAR TACHYCARDIA

Outcome of event

Event ID OUTC COD
4960036 DE

Reactions reported

Event ID PT
4960036 ACTINIC KERATOSIS
4960036 ACUTE SINUSITIS
4960036 BLOOD THYROID STIMULATING HORMONE INCREASED
4960036 BRONCHITIS
4960036 CARDIAC FAILURE CONGESTIVE
4960036 CARDIO-RESPIRATORY ARREST
4960036 CARDIOMYOPATHY
4960036 CONSTIPATION
4960036 DIZZINESS
4960036 FAECES DISCOLOURED
4960036 MYOCARDIAL INFARCTION
4960036 ONYCHOMYCOSIS
4960036 PALPITATIONS
4960036 PNEUMONIA
4960036 SINUS BRADYCARDIA
4960036 SINUSITIS
4960036 SUDDEN DEATH
4960036 TINEA PEDIS
4960036 UPPER RESPIRATORY TRACT INFECTION

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
4960036 1007118995 19990524 20000401 10 MON
4960036 1007118996 20000401 20010307
4960036 1007118997 19990524 20000401 10 MON
4960036 1007118998 20000401 20010307
4960036 1007119002 20000720