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2007-12-17 - Male

226568

Adverse reaction report number 226568
Latest AER version number 0
Market authorization holder AER number SPV1200705104
Initial received date 2007-12-17
Latest received date 2007-12-17
Age N/A
Gender Male
Weight N/A
Type of report Spontaneous
Reporter type Pharmacist
Source of report MAH
Report outcome Unknown
Serious report? No

Product information

Product description Dosage form Health product role Route of administration Dose Frequency Therapy duration Indication(s)
ADDERALL XRCAPSULE, EXTENDED RELEASESuspectOral7.5 Milligram every 1 Day(s)

Adverse reaction term information

MedDRA version: v.21.1
Adverse reaction terms Reaction duration
Drug ineffective
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