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Ultram overdose, contraindications and information tramadol

Ultram overdose. adverse events, including seizure and serotonin syndrome. Withdrawal Withdrawal symptoms may occur if ULTRAM is discontinued abruptly.(See DRUG ABUSE AND DEPENDENCE.) These symptoms may include: anxiety, sweating, insomnia, rigors, pain, nausea, tremors, diarrhea, upper respiratory symptoms, piloerection, and rarely hallucinations. Clinical experience suggests that withdrawal symptoms may be relieved by tapering the medication. Physical Dependence and Abuse ULTRAM may induce psychic and physical dependence of the morphine-type (µ-opioid) (see DRUG ABUSE AND DEPENDENCE). ULTRAM should not be used in opioid-dependent patients. ULTRAM has been shown to reinitiate physical dependence in some patients that have been previously dependent on other opioids. Dependence and abuse, including drug-seeking behavior and taking illicit actions to obtain the drug, are not limited to those patients with prior history of opioid dependence. Risk of Overdosage Serious potential consequences of overdosage ultram overdose
 

Ultram overdose, contraindications and information - tramadol hcl ...

with ULTRAM (tramadol hydrochloride tablets) are central nervous system depression, respiratory depression and death. In treating an overdose, primary attention should be given to maintaining adequate ventilation along with general supportive treatment (see OVERDOSAGE). PRECAUTIONS Acute Abdominal Conditions The administration of ULTRAM may complicate the clinical assessment of patients with acute abdominal conditions. Use in Renal and Hepatic Disease Impaired renal function results in a decreased rate and extent of excretion of tramadol and its active metabolite,M1.In patients with creatinine clearances of less than 30 mL min, dosing reduction is recommended (see DOSAGE AND ADMINISTRATION).Metabolism of tramadol and M1 is reduced in patients with advanced cirrhosis of the liver. In cirrhotic patients, dosing reduction is recommended (see DOSAGE AND ADMINISTRATION). With the prolonged half-life in these conditions, achievement of steady-state is delayed, so that it may take several da ultram overdose


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ultram overdose He rabbit. The dosages listed for mouse ultram overdose, rat and rabbit are 1.7 ultram overdose, 1.9 and 14.6 times the maximum daily human dosage (246 mg m2) ultram overdose, respectively. Non-teratogenic Effects Tramadol was evaluated in peri- and post-natal studies in rats. Progeny of dams receiving oral (gavage) dose levels of 50 mg kg (300 mg m2 or 1.2 times the maximum daily human tramadol dosage) or greater had decreased weights ultram overdose, and pup survival was decreased early in lactation at 80 mg kg (480 mg m2 or 1.9 and higher the maximum daily human dose). There are no adequate and well-controlled studies in pregnant women. ULTRAM should be used during pregnancy only if the potential benefit justifies the p ultram overdose.

ultram overdose Otential risk to the fetus. Neonatal seizures ultram overdose, neonatal withdrawal syndrome ultram overdose, fetal death and still birth have been reported during post-marketing. Labor and Delivery ULTRAM should not be used in pregnant women prior to or during labor unless the potential benefits outweigh the risks. Safe use in pregnancy has not been established. Chronic use during pregnancy may lead to physical dependence and post-partum withdrawal symptoms in the newborn (see DRUG ABUSE AND DEPENDENCE). Tramadol has been shown to cross the placenta. The mean ratio of serum tramadol in the umbilical veins compared to maternal veins was 0.83 for 40 women given tramadol during labor. The effect of ULTRAM ultram overdose, if any ultram overdose, on the later growth ultram overdose, development ultram overdose, and functional maturation of the child is unknown. Nursing Mothers ULTRAM is not recommended for obstetrical preoperative medication or for post-delivery analgesia in nursing mothers because its safety in infants and newborns has not been studied. Following a single IV 100 mg dose of tramadol ultram overdose, the cumulative excretion in breast milk within 16 hours postdose was 100 µg of tramadol (0.1% of the maternal dose) and 27 µg of M1. Pediatric Use The safety and efficacy of ULTRAM in patients under 16 years of age have not been established. The use of ULTRAM in the pediatric population is not recommended. Geriatr.

ultram overdose Ct of ULTRAM ultram overdose, if any ultram overdose, on the later growth ultram overdose, development ultram overdose, and functional maturation of the child is unknown. Nursing Mothers ULTRAM is not recommended for obstetrical preoperative medication or for post-delivery analgesia in nursing mothers because its safety in infants and newborns has not been studied. Following a single IV 100 mg dose of tramadol ultram overdose, the cumulative excretion in breast milk within 16 hours postdose was 100 µg of tramadol (0.1% of the maternal dose) and 27 µg of M1. Pediatric Use The safety and efficacy of ULTRAM in patients under 16 years of age have not been established. The use of ULTRAM in the pediatric population is not recommended. Geriatri.

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