Table 1.
Symptoms | Type of effect+ | Type of drug | |
---|---|---|---|
Synthetic Cannabinoids | Cannabis | ||
Neuropsychiatric | Acute | Severe psychotic symptoms including; agitation (28), aggression, catatonia, paranoia, auditory and visual hallucinations, perceptual alterations, and persistent psychosis episode (10, 14, 29). | Perceptual alterations including; hallucinations and distortion of spatial perception are typical effects (7, 30). Paranoia, aggressiveness, and prolonged psychosis were observed in vulnerable users and are dose-related (1, 2, 7). |
Long-term | Chronic use may increase the risk for developing psychotic disorders (15, 27, 31). | An increased risk of psychotic disorders in vulnerable individuals and naïve users (2, 25, 27, 32). | |
Affect | Acute | Negative mood, panic attacks, manic behavior (13), depression (16), and suicidal ideation (10, 33). | Anxiety and panic attacks; especially in naïve users (1). |
Long-term | Depression (16), irritability and persistent anxiety (29, 33). | An increased risk for developing anxiety (34, 35), and mood disorders (1, 36, 37). | |
Cognitive | Acute | Severe cognitive impairments including; memory alteration, attention difficulties, and amnesia (13, 33). | Wide range of dose-related cognitive deficits including; attention, working-memory, cognitive inhibition, and psychomotor function (38–41). |
Long-term | Executive function deficits of working memory and attention (16) | Impairments of set-shifting, verbal learning, attention, short-term memory and psychomotor functions (39, 42). | |
Cardiovascular | Acute | Tachycardia, hypertension, myocardial infraction, arrhythmias, chest pain, and palpitations (13, 43). | An increase of cardiovascular activity, increase heart rate, and decrease blood pressure (44, 40). |
Long-term | Prolong use may increase risk of cardiovascular disease (44, 45). | An increased risk of cardiovascular disease after prolong use (1, 44, 46). | |
Neurologic | Acute | Dizziness, somnolence, seizures, hypertonicity, hyperflexion, hyperextension, sensation changes, and fasciculations (10, 14, 29). | Dizziness, somnolence, and muscle tension (38, 40). |
Long-term | Preliminary evidence for structural and functional central nervous system alterations (47, 48). | Structural and functional abnormalities in a range of brain areas including the hippocampus and amygdala (49, 50). | |
Gastrointestinal | Acute | Nausea, emesis, and appetite change (10, 14, 20, 29). | Hyperemesis, and increase appetite (1, 7, 20). |
Long-term | Severe weight-loss after prolong use (10, 13). | Low body weight among regular users (51). | |
Other | Acute | Acute kidney injury, abdominal pain, miosis, mydriasis, xerostomia, hyperthermia, fatigue, rhabdomyolysis, cough (11, 13, 43), deficits of driving ability (52, 53, 54). | Bronchodilation (55), impairments of driving ability (1, 7). |
Long-term | Kidney diseases, insomnia, nightmares, dependency, tolerance, and withdrawal (11, 13, 43). | An increased risk of obstructive lung disease including lung-cancer (1, 7, 55), an increased risk of cancers of the oral cavity, pharynx and esophagus (56), cannabis addiction, tolerance, and withdrawal (1, 7). |
Acute effect denotes 0–6 h after last drug use; Long-term effects denotes 3 weeks or longer after last drug use.