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thiothixene (Navane)

 

Classes: Antipsychotics, 1st Generation

Dosing and uses of Navane (thiothixene)

 

Adult dosage forms and strengths

capsule

  • 1mg
  • 2mg
  • 5mg
  • 10mg

 

Schizophrenia

Mild-Moderate: initial: 2 mg PO q8hr; may increase to 15 mg/day

Severe: initial 5 mg PO q12hr

Maintenance: 20-30 mg/day; no more than 60 mg/day PO divided q8-12hr

 

Pediatric dosage forms and strengths

capsule

  • 1mg
  • 2mg
  • 5mg
  • 10mg

 

Schizophrenia

<12 years

  • Not recommended

>12 years

  • Mild-Moderate: initial: 2 mg PO q8hr; may increase to 15 mg/day
  • Severe: initial 5 mg PO q12hr
  • Maintenance: 20-30 mg/day; no more than 60 mg/day PO divided q8-12hr

 

Navane (thiothixene) adverse (side) effects

Frequency not defined

Constipation

Decr sweating

Drowsiness

EPS ( muscle stiffness, dystonia, Parkinsonism, tardive dyskinesia, akathisia) (60%)

Incr appetite

Orthostatic hypotension

Photosensitivity

Wt gain

Xerostomia

Agitation

Allergic dermatitis

Allergic reactions

Anorexia

Anticholinergic effects

Anxiety

Cerebral edema

Depression

Dizziness

Erectile dysfunction

Euphoria

Headache

Ileus

Insomnia

Irregular menses

Lens opacities (prolonged use)

Poikilothermia

Rash

Restlessness

Sedation

Tachycardia

Weakness

Agranulocytosis, blood dyscrasias (rare)

Galactorrhea (rare)

Heat stroke (rare)

NMS (infrequent but serious)

Obstructive hyperbilirubinemia (rare)

Cholestatic jaundice

Confusion

Decr gag reflex

Gynecomastia

Hyperpyrexia

Peripheral edema

 

Warnings

Black box warnings

Patients with dementia-related psychosis who are treated with antipsychotic drugs are at an increased risk of death as shown in short-term controlled trials. The deaths appeared to be either cardiovascular (eg, heart failure, sudden death) or infectious (eg, pneumonia) in nature.

This drug is not approved for the treatment of patients with dementia-related psychosis.

 

Contraindications

Documented hypersensitivity

Blood dyscrasias

Coma

Circulatory collapse

CNS depression (including coma)

Neuroleptic malignant syndrome (NMS)

Poorly controlled seizure disorder

Breastfeeding

 

Cautions

Alcohol withdrawal, cardiovascular disease, glaucoma, BPH, history of seizure disorder, Parkinsonism, urinary retention, liver disease

Potential cross sensitivity between thioxanthenes & phenothiazine derivatives

FDA Warning regarding off-label use for dementia in elderly

Leukopenia/neutropenia and agranulocytosis reported; possible risk factors for leukopenia/neutropenia include pre-existing low white blood cell count (WBC) and history of drug-induced leukopenia/neutropenia

If history of clinically significant low WBC or drug-induced leukopenia/neutropenia, monitor complete blood count (CBC) frequently during first few months of therapy; discontinue drug at first sign of a clinically significant decline <1000/mm³ in WBC in absence of other causative factors and continue monitoring WBC until recovery

 

Pregnancy and lactation

Pregnancy category: C

Neonates exposed to antipsychotic drugs during the 3rd trimester of pregnancy are at risk for extrapyramidal and/or withdrawal symptoms following delivery

These complications vary in severity; in some cases, symptoms have been self-limited, while in other cases neonates have required intensive care unit support and prolonged hospitalization

Lactation: may be excreted in breast milk; not advised

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Navane (thiothixene)

Mechanism of action

Thioxanthene; dopamine D2 receptor antagonist; may also have anticholinergic and alpha-blocking effects

 

Pharmacokinetics

Half-life elimination: 24 hr

Metabolism: Liver (CYP1A2)

Protein bound: 90%