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
7584282 7970889 F 7584282-3 20110319 20110627 20110630 EXP US-MYLANLABS-2011S1010760 MYLAN PHARMACEUTICALS INC. 48 YR F Y 59.88 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
7584282 1016907183 C MIDODRINE HYDROCHLORIDE 1 ORAL
7584282 1016907185 C CALTRATE + VITAMIN D 2
7584282 1016907186 C CLONAZEPAM 1
7584282 1016907181 SS LEVETIRACETAM 1 ORAL 076919
7584282 1016907184 C FIORICET 1 ORAL 50MG/325MG/40MG
7584282 1016907179 SS LEVETIRACETAM 1 ORAL 076919
7584282 1016907178 PS LEVETIRACETAM 1 ORAL 076919
7584282 1016907180 SS LEVETIRACETAM 1 ORAL 076919
7584282 1016907182 SS LEVETIRACETAM 1 ORAL 076919

Indications of drugs used

Event ID DRUG SEQ INDI PT
7584282 1016907183 HYPOTENSION
7584282 1016907184 MIGRAINE
7584282 1016907178 CONVULSION

Outcome of event

Event ID OUTC COD
7584282 HO
7584282 OT

Reactions reported

Event ID PT
7584282 CONCUSSION
7584282 EYE SWELLING
7584282 CONTUSION
7584282 INJURY
7584282 ELECTROENCEPHALOGRAM ABNORMAL
7584282 DRUG INEFFECTIVE FOR UNAPPROVED INDICATION
7584282 CONVULSION
7584282 GRAND MAL CONVULSION
7584282 LOSS OF CONSCIOUSNESS

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
7584282 1016907183 20081001 20110505
7584282 1016907181 20110105 20110505
7584282 1016907184 20100101 20110505
7584282 1016907179 20101201 20110105
7584282 1016907178 20101101 20101201
7584282 1016907180 20101201 20110105
7584282 1016907182 20110105 20110505