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2018-11-21 - Male

720527

Adverse reaction report number 720527
Latest AER version number 0
Market authorization holder AER number 632971
Initial received date 2018-11-21
Latest received date 2018-11-21
Age N/A
Gender Male
Weight N/A
Type of report Spontaneous
Reporter type Other Health Professional
Source of report MAH
Report outcome Unknown
Serious report? Yes

Reason for seriousness

Death
Disability
Cogenital anomaly
Life threateting
Hospitalization Yes
Other medically important

Product information

Product description Dosage form Health product role Route of administration Dose Frequency Therapy duration Indication(s)
OZEMPICSOLUTION SUBCUTANEOUSSuspectSubcutaneous1 Milligram1 every 1 Week(s) Product used for unknown indication

Adverse reaction term information

MedDRA version: v.21.1
Adverse reaction terms Reaction duration
Nausea
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