| Literature DB >> 28449569 |
Soumitra Ghosh1, Dhrubajyoti Bhuyan1.
Abstract
Baclofen is a gamma-aminobutyric acid type B receptor agonist used as an anti-craving agent for treatment of alcohol dependence. It has gained popularity in the recent times because it is well tolerated even in patients with hepatic impairments. Herein we are summarizing the latest literature about baclofen induced hypomania and are reporting a case of baclofen abuse because of its mood elevating property in a patient of alcohol dependence with comorbid major depressive disorder. Literature review and case study of a 36-year-old male with alcohol dependence with comorbid major depressive disorder was prescribed with tablet baclofen as an anti-craving agent along with antidepressant medicines. The patients who did not improve with conventional antidepressant therapy started feeling better in terms of his mood symptoms on taking tablet baclofen. Owing to the mood elevating property he started abusing baclofen. Despite its safety profile in hepatic impairment, one must be very cautious in prescribing baclofen because of its mood altering property which may account for its abuse potentiality.Entities:
Keywords: Alcoholism; Baclofen; Baclofen abuse; Treatment-resistant depressive disorder
Year: 2017 PMID: 28449569 PMCID: PMC5426491 DOI: 10.9758/cpn.2017.15.2.187
Source DB: PubMed Journal: Clin Psychopharmacol Neurosci ISSN: 1738-1088 Impact factor: 2.582
The Naranjo adverse drug reaction probability scale and its responses
| The Naranjo adverse drug reaction probability scale; To assess the adverse drug reaction, please answer the following questionnaire and give the pertinent score | Yes | No | Do not know | Score |
|---|---|---|---|---|
| 1. Are there previous | +1 | 0 | 0 | +1 |
| 2. Did the adverse event occur after the suspected drug was administered? | +2 | −1 | 0 | +2 |
| 3. Did the adverse reaction improve when the drug was discontinued or a | +1 | 0 | 0 | +1 |
| 4. Did the adverse reaction reappear when the drug was re-administered? | +2 | −1 | 0 | +2 |
| 5. Are there alternative causes (other than the drug) that could have on their own caused the reaction? | −1 | +2 | 0 | −1 |
| 6. Did the reaction reappear when a placebo was given? | −1 | +1 | 0 | 0 |
| 7. Was the blood detected in the blood (or other fluids) in concentrations known to be toxic? | +1 | 0 | 0 | 0 |
| 8. Was the reaction more severe when the dose was increased or less severe when the dose was decreased? | +1 | 0 | 0 | +1 |
| 9. Did the patient have a similar reaction to the same or similar drugs in | +1 | 0 | 0 | +1 |
| 10. Was the adverse event confirmed by any objective evidence? | +1 | 0 | 0 | 0 |
| Total | 7 |
The adverse drug reaction is assigned to a probability category from the total score as follows: definite if the overall score is 9 or greater, probable for a score of 5–8, possible for 1–4 and doubtful if the score is 0.15)