Precautions:
Before you use Prodep 60, tell your doctor if you are allergic to it or its ingredients. Your doctor may prescribe an alternative medicine and update your medical records to record this information.
Before you use Prodep 60 Capsule, tell your doctor of your medical history including treatments such as triptans, tricyclics, lithium, selective serotonin reuptake inhibitors (SSRIs), serotonin and norepinephrine reuptake inhibitors (SNRIs), monoamine oxidase inhibitors (MAOIs), antipsychotics, tramadol, fentanyl, amphetamines, tryptophan or St. John’s Wort, electroconvulsive therapy (ECT), liver problems, kidney problems, heart problems, seizures, abnormal mood state (mania), low sodium level in the blood, stroke, bleeding problems, high blood pressure, prolonged or irregular heartbeat, or suicidal thoughts. Patients taking certain drugs with Prodep 60 may affect the metabolism of Prodep 60 which may lead to serotonin syndrome symptoms such as agitation, hallucinations, coma, increased heartbeat, abnormal blood pressure, dizziness, increased sweating, flushing, and fever. Prolonged seizures may be observed in patients taking electroconvulsive therapy (ECT) along with Prodep 60 therapy. In patients with liver and kidney problems, Prodep 60 may not be able to properly metabolized and excreted from the body which may lead to accumulation of metabolites into the body. Patient with a history of a heart problem such as QT prolongation may at an increased risk of abnormal heartbeat while using Prodep 60. Use of Prodep 60 in patients with the history of mania may increase the risk of developing an elevated and unusually irritable mood behavior (mixed/manic episode). Patients taking Prodep 60 with the history of bleeding disorders are at an increased risk of developing discoloration of the skin, solid blood clot swelling, nose bleeding and rupturing of blood vessels.
The use of this medicine may change height and weight. The children may experience possible slowed growth rate and weight change during Prodep 60 therapy.
The use of Prodep 60 Capsule may change ECG monitoring. The patients may experience prolonged heartbeat and increased and decreased heartbeat during Prodep 60 therapy.
Consult with your doctor on the use of Prodep 60 Capsule during pregnancy or if you are planning to become pregnant. Use of Prodep 60 late in the third trimester may cause complications in newborn which include breathing problem during sleep (apnea), respiratory distress, seizures, bluish or purplish skin discoloration (cyanosis), temperature instability, muscle weakness (hypotonia), feeding difficulty, muscle rigidity (hypertonia), vomiting, low blood sugar (hypoglycemia), overactive response (hyperreflexia), tremor, involuntary movements (jitteriness), constant crying, irritability. Prodep 60 should only be used in pregnancy if potential benefits of medicine justify the possible risks. Consult with your doctor on the use of Prodep 60 Capsule during breastfeeding. Prodep 60 may pass into the breast milk and may cause side effects in babies. Discontinuation of breastfeeding should be considered if treatment with Prodep 60 is required. If breastfeeding is required in the baby, the lower effective dose of Prodep 60 should be considered. Consult with your doctor on the use of Prodep 60 Capsule, if you are trying to conceive.