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
7488573 7317689 F 7488573-6 20090301 20110412 20110518 EXP US-BAYER-201016048NA BAYER HEALTHCARE PHARMACEUTICALS INC. 36 YR F Y 75.737 KG 20110518 OT 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
7488573 1016530344 SS YASMIN 1 ORAL UNK UNK, QD
7488573 1016530345 C BUTALBITAL 1 UNK
7488573 1016530350 C NAPROSYN 1
7488573 1016530346 C FLUOXETINE 1 UNK
7488573 1016530349 C FIORICET 1 UNK
7488573 1016530343 PS YAZ 1 ORAL UNK UNK, QD 021676
7488573 1016530347 C OMEPRAZOLE 1 UNK
7488573 1016530348 C XANAX 1 0.25 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
7488573 1016530345 MIGRAINE
7488573 1016530350 MIGRAINE
7488573 1016530346 DEPRESSION
7488573 1016530349 MIGRAINE
7488573 1016530343 CONTRACEPTION
7488573 1016530347 GASTROOESOPHAGEAL REFLUX DISEASE
7488573 1016530348 ANXIETY

Outcome of event

Event ID OUTC COD
7488573 OT

Reactions reported

Event ID PT
7488573 HIATUS HERNIA
7488573 OESOPHAGEAL INJURY
7488573 CHOLECYSTECTOMY
7488573 OESOPHAGITIS
7488573 INJURY
7488573 MENTAL DISORDER

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
7488573 1016530345 20050101 20100101
7488573 1016530346 20100101
7488573 1016530349 20071001
7488573 1016530343 20080101 20090101
7488573 1016530347 20090101 20100101
7488573 1016530348 20070301