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. 2017 Sep 6;10(4):407–419. doi: 10.1159/000478098

Table 4.

Total ADRs for each treatment group and ADRs leading to drop out of patients before the end of the study

ADR Placebo 16 mg cathine 32 mg cathine 53.3 mg cathine
Tachycardia 2
Palpitations 5
Chest pain 2
Hypertension 1 1 3
Ischemia 1
Ventricular extrasystoles 1
ECG QT prolonged 1
Dizziness 1
Syncope 1
Headache 1 1 1
Restlessness 1 1 1 3
Psychomotor hyperactivity 1
Sleep disorder 1 1
Depression 1 1
Panic attack 1
Hot flush 3
Dry mouth 2 2
Hyperhidrosis 2
Hepatic enzyme increased 1
Transaminases increased 1
GGT increased 1
Blood glucose increased 1
Hyperglycemia 1
Weight increased 1
Muscle spasms 1 1
Hypersensitivity 1
Leukopenia 1 2
Peripheral coldness 1
Constipation 1
Paresthesia 1
Thirst 1
Erectile dysfunction 1
Total reported ADRs 9 11 14 26
Drop outs due to an ADR 3a 3b 4c 2d
a

1× headache, 1× depression, 1× hyperglycemia.

b

1× dizziness, 1× GGT increased, 1× hypersensitivity.

c

1× sleep disorder, 1× hot flush, 1× hepatic enzyme increased, 1× transaminases increased.

d

1× ischemia, 1× dry mouth.