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
7584281 8017338 I 7584281-1 19960401 20110624 20110630 EXP US-MYLANLABS-2011S1013228 MYLAN PHARMACEUTICALS INC. 42 YR F Y 104.33 KG 20110630 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
7584281 1016907175 SS AMITRIPTYLINE HCL 1 ORAL 086009
7584281 1016907176 SS LEVBID 2 ORAL
7584281 1016907172 SS XANAX 1 ORAL
7584281 1016907173 SS TIGAN 1 ORAL
7584281 1016907174 PS ELAVIL 1 086009
7584281 1016907177 SS HYOMAX 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
7584281 1016907175 IRRITABLE BOWEL SYNDROME
7584281 1016907176 NAUSEA
7584281 1016907172 IRRITABLE BOWEL SYNDROME
7584281 1016907173 NAUSEA
7584281 1016907174 IRRITABLE BOWEL SYNDROME
7584281 1016907177 NAUSEA

Outcome of event

Event ID OUTC COD
7584281 DS
7584281 OT

Reactions reported

Event ID PT
7584281 INSOMNIA
7584281 MENTAL IMPAIRMENT
7584281 SINUSITIS
7584281 DISTURBANCE IN ATTENTION
7584281 HYPERTENSION
7584281 BREAST CANCER
7584281 NAUSEA
7584281 FIBROMYALGIA
7584281 HYPERVENTILATION

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
7584281 1016907175 19930101
7584281 1016907176 19930101
7584281 1016907172 19930101
7584281 1016907174 19930101 19930101