Specific codes in ICD-10 are unique alphanumeric designations used to identify and categorize diseases, disorders, and conditions. They consist of 3-5 characters, including both letters and numbers, that provide a high level of detail and specificity.
| Language | Translation |
|---|---|
English
|
Mental and behavioural disorders due to use of sedatives or hypnotics |
French
|
Troubles mentaux et du comportement liés à l'utilisation de sédatifs ou d'hypnotiques |
| Level | Code | Title | |
|---|---|---|---|
| 1 | V | Mental and behavioural disorders | |
| 2 | F10-F19 | Mental and behavioural disorders due to psychoactive substance use | |
| 3 | F13 | Mental and behavioural disorders due to use of sedatives or hypnotics |
| Code | Title | |
|---|---|---|
| F13.0 | Acute intoxication | |
| F13.1 | Harmful use | |
| F13.2 | Dependence syndrome | |
| F13.3 | Withdrawal state | |
| F13.4 | Withdrawal state with delirium | |
| F13.5 | Psychotic disorder | |
| F13.6 | Amnesic syndrome | |
| F13.7 | Residual and late-onset psychotic disorder | |
| F13.8 | Other mental and behavioural disorders | |
| F13.9 | Unspecified mental and behavioural disorder |
| Active Ingredient | Description | |
|---|---|---|
| Citalopram |
Citalopram is the most Selective Serotonin Reuptake Inhibitor (SSRI) yet described, with no, or minimal, effect on noradrenaline (NA), dopamine (DA) and gamma aminobutyric acid (GABA) uptake. |
|
| Penfluridol |
|
|
| Pimozide |
Pimozide is an orally active neuroleptic drug which blocks central dopaminergic receptors. Pimozide antagonises many of the actions of amphetamine and apomorphine. |
|
| Pipamperone |
|
|
| Sulpiride |
Sulpiride is a member of the group of substituted benzamides, which are structurally distinct from the phenothiazines, butyrophenones and thioxanthenes. One of the characteristics of sulpiride is its bimodal activity, as it has both antidepressant and neuroleptic properties. Schizophrenia characterised by a lack of social contact can benefit strikingly. |
|
| Tiapride |
Tiapride is an atypical neuroleptic which exhibits selectivity in in-vitro studies for D2 and D3 dopamine subtype receptors without any affinity for subtype receptors of the principal central neurotransmitters (including serotonin, noradrenaline and histamine). |
|
| Trazodone |
Trazodone is a potent antidepressant. It also has anxiety reducing activity. Trazodone is a triazolopyridine derivative chemically unrelated to known tricyclic, tetracyclic and other antidepressant agents. It has negligible effect on noradrenaline re-uptake mechanisms. |
|
| Trifluoperazine |
Trifluoperazine is one of the phenothiazine class of compounds and as such has many pharmacodynamic effects which relate to its therapeutic actions and side effects. The most notable action of phenothiazines is antagonism at dopamine receptors in the CNS. |
