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
8248788 8468426 F 8248788-6 20120201 20120322 20120331 EXP JP-ALLERGAN-1203795US ALLERGANFDA 20 YR F Y 20120331 MD JAPAN

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
8248788 1019282894 SS BOTOX 1 INTRAMUSCULAR 30 UNITS, LEFT SPLENIUS MUSCLE
8248788 1019282895 SS BOTOX 1 INTRAMUSCULAR 30 UNITS, RIGHT SPLENIUS MUSCLE
8248788 1019282896 SS BOTOX 1 INTRAMUSCULAR 30 UNITS, TRAPEZIUS MUSCLE
8248788 1019282893 SS BOTOX 1 INTRAMUSCULAR 30 UNITS, RIGHT TRAPEZIUS MUSCLE
8248788 1019282897 C DEPAKENE 1 ORAL 3 SEPARATE DOSES PER DAY
8248788 1019282900 C TIZANIDINE HCL 1 ORAL 3 SEPERATE DOSES PER DAY
8248788 1019282892 PS BOTOX 1 INTRAMUSCULAR 10 UNITS, LEFT STERNOCLEIDOMASTOID MUSCLE
8248788 1019282898 C DIAMOX 1 ORAL 3 SEPARATE DOSES PER DAY
8248788 1019282899 C NITRAZEPAM 1 ORAL 3 SEPERATE DOSES PER DAY

Indications of drugs used

Event ID DRUG SEQ INDI PT
8248788 1019282897 PRODUCT USED FOR UNKNOWN INDICATION
8248788 1019282900 PRODUCT USED FOR UNKNOWN INDICATION
8248788 1019282892 TORTICOLLIS
8248788 1019282898 PRODUCT USED FOR UNKNOWN INDICATION
8248788 1019282899 PRODUCT USED FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
8248788 HO

Reactions reported

Event ID PT
8248788 PNEUMONIA

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
8248788 1019282894 20120127 20120127 1 DAY
8248788 1019282896 20120127 20120127 1 DAY
8248788 1019282893 20120127 20120127 1 DAY
8248788 1019282892 20120127 20120127 1 DAY