sociated with diabetic neuropathy in the combined LYRICA group for which the incidence was greater in this combined LYRICA group than in the placebo group. A majority of pregabalin-treated patients in clinical studies had adverse reactions with a maximum intensity of "mild" or "moderate".
	Table 3. Treatment-emergent adverse reaction incidence in controlled trials in neuropathic pain associated with diabetic peripheral neuropathy (events in at least 1% of all LYRICA-treated patients and at least numerically more in all LYRICA than in the placebo group)
	Body system
	Preferred term 75 mg/day
	[N=77]
	% 150 mg/day
	[N=212]
	% 300 mg/day
	[N=321]
	% 600 mg/day
	[N=369]
	% All PGB* Placebo
	[N=979]
	% [N=459]
	%
	* PGB: pregabalin † Thinking abnormal primarily consists of events related to difficulty with concentration/attention but also includes events related to cognition and language problems and slowed thinking. ‡ Investigator term; summary level term is amblyopia
	Body as a whole
	Asthenia 4 2 4 7 5 2
	Accidental injury 5 2 2 6 4 3
	Back pain 0 2 1 2 2 0
	Chest pain 4 1 1 2 2 1
	Face edema 0 1 1 2 1 0
	Digestive system
	Dry mouth 3 2 5 7 5 1
	Constipation 0 2 4 6 4 2
	Flatulence 3 0 2 3 2 1
	Metabolic and nutritional disorders
	Peripheral edema 4 6 9 12 9 2
	Weight gain 0 4 4 6 4 0
	Edema 0 2 4 2 2 0
	Hypoglycemia 1 3 2 1 2 1
	Nervous system
	Dizziness 8 9 23 29 21 5
	Somnolence 4 6 13 16 12 3
	Neuropathy 9 2 2 5 4 3
	Ataxia 6 1 2 4 3 1
	Vertigo 1 2 2 4 3 1
	Confusion 0 1 2 3 2 1
	Euphoria 0 0 3 2 2 0
	Incoordination 1 0 2 2 2 0
	Thinking abnormal† 1 0 1 3 2 0
	Tremor 1 1 1 2 1 0
	Abnormal gait 1 0 1 3 1 0
	Amnesia 3 1 0 2 1 0
	Nervousness 0 1 1 1 1 0
	Respiratory system
	Dyspnea 3 0 2 2 2 1
	Special senses
	Blurry vision‡ 3 1 3 6 4 2
	Abnormal vision 1 0 1 1 1 0
	Controlled Studies in Postherpetic Neuralgia
	Adverse Reactions Leading to Discontinuation
	In clinical trials in patients with postherpetic neuralgia, 14% of patients treated with LYRICA and 7% of patients treated with placebo discontinued prematurely due to adverse reactions. In the LYRICA treatment group, the most common reasons for discontinuation due to adverse reactions were dizziness (4%) and somnolence (3%). In c