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
5478536 6211153 I 5478536-4 20061117 20061225 20070109 EXP US-KINGPHARMUSA00001-K200601628 KINGPHARMUSA00001 Y 20070109 CN FRANCE

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
5478536 1009012185 PS ALTACE 1 ORAL 1.25 MG, TID 019901
5478536 1009012186 SS LASIX 1 ORAL 40 MG, BID
5478536 1009012187 SS ALDACTAZIDE 1 1 U, QD
5478536 1009012188 C DIPIPERON 2 ORAL 80 MG, UNK
5478536 1009012189 C PREVISCAN /00789001/ 2 ORAL 10 MG, UNK
5478536 1009012190 C IMOVANE 2 ORAL 3.75 MG, UNK
5478536 1009012191 C TRAMADOL HCL 1 ORAL 200 MG, UNK
5478536 1009012192 C SERETIDE /01420901/ 2
5478536 1009012193 C MOTILYO 2 ORAL 4 U, UNK

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5478536 HO

Reactions reported

Event ID PT
5478536 ABNORMAL BEHAVIOUR
5478536 AGGRESSION
5478536 DEHYDRATION
5478536 DRUG INTERACTION
5478536 FALL
5478536 HYPOTENSION
5478536 HYPOTHERMIA
5478536 MALAISE
5478536 RENAL FAILURE ACUTE
5478536 TRAUMATIC HAEMATOMA
5478536 WOUND

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
5478536 1009012186 20061117
5478536 1009012187 20061117
5478536 1009012190 20061117