Patients with mental illness
Alprox should not be as a primary treatment of mental illness.
Risk of harm in an unborn baby
Pregnant women taking Alprox may have an increased risk of harm to the unborn baby. This medicine may cause birth defects to unborn babies when given to pregnant women in their first trimester. Alprox should be avoided in the first 12 weeks of pregnancy
. If patients are taking Alprox, become pregnant or plan to pregnant during treatment they should consult with their doctor about taking or discontinuing the drug.
The repeated use of Alprox for few weeks may cause a decrease in its sleep-inducing effect.
The use of Alprox in patients with depression
are at increased risk. The use of Alprox in patients with depression may cause periods of mild to moderate abnormally elevated mood.
Slow down of body activities (CNS depression)
Alprox may cause slow down of body activities due to its brain depressive
effect. Patients taking Alprox should be cautioned while doing activities which require full mental alertness such as driving a motor vehicle or operating
machinery. Such patients also should be cautioned about the simultaneous consumption of alcohol
and other brain depressive drugs.
Depression or anxiety
Patients with depression
are at an increased risk when taking this medicine. Such patients may have increased risk of suicide
when they take Alprox alone. Alprox should be given for a short period with caution in patients with symptoms of depression or suicide.
Elderly patients are at an increased risk when taking this medicine. Such patients may have an increased risk of muscle weakness, severe respiratory insufficiency, and sleepiness. Alprox should be given with caution and start with a low dose in such patients.
Patients taking Alprox
Patients using Alprox may have a risk of withdrawal symptoms including prolonged seizures
that can be possibly fatal.
Symptoms occur between dose intervals
Patients using Alprox may have a risk of early morning anxiety
which may indicate the development of tolerance. The same total daily dose of Alprox should be given in divided doses to such patients.
Risk of dose reduction
The reduction of dose in patients using Alprox may have a risk of withdrawal reactions. The doses of Alprox should be decreased and stopped gradually.
Use of opioids
Patients using Alprox with opioids
are at an increased risk. Such patients may have an increased risk of sleepiness, coma
, breathing problems, and can be fatal. A lowest effective dose of Alprox should be given for the minimum duration of time with opioids. Closely monitor signs and symptoms of breathing problems and sleepiness. It is also advised to patients not to drive or operate heavy machinery.
Dependence and withdrawal reactions
There is a risk of dependence and withdrawal reactions in patients who are using Alprox. This may occur in patients with a history of alcohol
use or misuse of the drug. Patients using Alprox may have a risk of dependence to Alprox which can be life-threatening. This medicine also causes withdrawal symptoms including seizures
, disturbed focus, abnormal sensation, inability to think clearly or concentrate (clouded sensorium), weight loss, heightened sensory perception, appetite decrease, alteration of the perception of smell (dysosmia), blurred vision, muscle cramps
, and muscle twitch. Alprox should be discontinued by reducing dosage slowly. The dosage of Alprox may be decreased by no more than 0.5 mg every three days.
Memory loss (amnesia)
Patients taking Alprox are at an increased risk of memory
loss. The patients should take continuous 7 to 8 hours sleep to reduce the risk of memory loss.
Mental and drug-related reactions (psychiatric and paradoxical reactions)
Children and elderly patients are at an increased risk when using this medicine. Such patients may have an increased risk of nervousness, restlessness, irritability, delusion, aggressiveness, violent uncontrollable anger, nightmares, inappropriate behavior, severe mental disorder, and hallucinations
. The use of Alprox in such patients should be discontinued.
Abnormal functioning of kidneys and liver
Patients with abnormal functioning of kidneys and liver are at an increased risk. Alprox should be given with caution in such patients.