The Safety Rates Drug Report

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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
6591998 7286999 F 6591998-4 20091006 20100221 EXP US-ALLERGAN-0911675US ALLERGANFDA 65 YR M Y 74.83 KG 20100221 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
6591998 1013160597 PS BOTOX 1 INTRAMUSCULAR 200 UNITS, SINGLE
6591998 1013160598 SS BOTOX 1 60 UNITS, SINGLE

Indications of drugs used

Event ID DRUG SEQ INDI PT
6591998 1013160597 HEADACHE

Outcome of event

Event ID OUTC COD
6591998 OT

Reactions reported

Event ID PT
6591998 MUSCULAR WEAKNESS
6591998 NECK PAIN

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
6591998 1013160597 20090728 20090728 1 DAY
6591998 1013160598 20010101 20010101 1 DAY