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
4960038 5972574 F 4960038-2 20001101 20050607 20060331 EXP US-MERCK-0506USA01067 MERCK HUMAN HEALTH DIVISION 58 YR F Y 64 KG 20060403 MD 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
4960038 1007119005 PS VIOXX 1 ORAL 21042
4960038 1007119006 C TYLENOL (CAPLET) 1 UNKNOWN
4960038 1007119007 C EFFEXOR 1 UNKNOWN
4960038 1007119008 C SYNTHROID 1 UNKNOWN
4960038 1007119009 C ZOCOR 1 UNKNOWN
4960038 1007119010 C RESTORIL 1 UNKNOWN
4960038 1007119011 C MONOPRIL 1 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
4960038 1007119005 PAIN

Outcome of event

Event ID OUTC COD
4960038 HO
4960038 OT

Reactions reported

Event ID PT
4960038 ACCELERATED HYPERTENSION
4960038 ACUTE PRERENAL FAILURE
4960038 ARTHRITIS
4960038 BACK PAIN
4960038 CARPAL TUNNEL SYNDROME
4960038 CEREBRAL INFARCTION
4960038 CHEST PAIN
4960038 CONVULSION
4960038 DEAFNESS NEUROSENSORY
4960038 DEPRESSION
4960038 DRUG HYPERSENSITIVITY
4960038 ENDOMETRITIS
4960038 FIBROMYALGIA
4960038 HEAD BANGING
4960038 HEADACHE
4960038 HEPATIC MASS
4960038 HYPERCHOLESTEROLAEMIA
4960038 HYPERLIPIDAEMIA
4960038 HYPERTENSIVE ENCEPHALOPATHY
4960038 MEMORY IMPAIRMENT
4960038 MYOFASCIAL PAIN SYNDROME
4960038 ORTHOSTATIC HYPOTENSION
4960038 OSTEOARTHRITIS
4960038 PAIN
4960038 POST-TRAUMATIC STRESS DISORDER
4960038 RENAL CYST
4960038 RESTLESS LEGS SYNDROME
4960038 ROAD TRAFFIC ACCIDENT
4960038 TENDONITIS

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
4960038 1007119005 19990501 20040901