Atomoxetine (StratteraĦ): increases in blood pressure and heart rate

What is Strattera?

Atomoxetine or Strattera Medication Information (dosing, side effects, patient counseling)

Straterra and high blood pressure

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Strattera atomoxetine straterra and high blood pressure a selective norepinephrine reuptake inhibitor prescribed for treating attention deficit hyperactivity disorder ADHD. Strattera is available as a generic drug. Common side effects of Strattera include: Tell your doctor if you have serious side effects of Strattera including: Strattera may interact with albuterolamiodaronestraterra and high blood pressure, bupropioncelecoxib, cimetidinedoxorubicinmethadonestraterra and high blood pressurequinidine, ritonavir, ranitidineterbinafineantidepressantsantihistaminesor sleep medicines.

Tell your doctor all medication and supplements you use, straterra and high blood pressure. Strattera may cause severe liver injury. There are no adequate studies of Strattera in pregnant women and it is not known if Strattera is secreted in human breast milk.

Tell your doctor if you are pregnant or plan to become pregnant or if you are breastfeeding before using Strattera. Our Strattera Side Effects Drug Center provides a comprehensive view of available drug information on the potential side straterra and high blood pressure when taking this medication. This is not a complete list of side effects and others may occur.

Call your doctor for medical advice about side effects. Get emergency medical help if you have signs of an allergic reaction: Report any new or worsening symptoms to your doctorsuch as: Atomoxetine can affect growth in children.

Tell your doctor if your child is not growing at a normal rate while using this medicine. Read straterra and high blood pressure entire detailed patient monograph for Strattera Atomoxetine HCl. During the ADHD clinical trials, children and adolescent patients were treated for longer than 1 year and children and adolescent patients were treated for over 6 months.

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. In acute child and adolescent placebo-controlled trials, 3. For all studies, including open-label and long-term studies6.

In the clinical development program, seizures were reported in 0. In these clinical trials, the seizure risk among poor metabolizers was 0. The following reactions did not meet this criterion but were reported by more atomoxetine-treated patients than placebo-treated patients and are possibly related to atomoxetine treatment: The following reaction did not meet this criterion but shows a statistically significant dose relationship: In the acute adult placebo-controlled trials, In the clinical development program, seizures were reported on 0.

Atomoxetine appears to impair sexual function in some patients. Changes in sexual desire, sexual performance, and sexual satisfaction are not well assessed in most clinical trials because they need special attention and because patients and physicians may be reluctant to discuss them.

Accordingly, estimates of the incidence of untoward sexual experience and performance cited in product labeling are likely to underestimate the actual incidence, straterra and high blood pressure. While it is difficult to know the precise risk of sexual dysfunction associated with the use of STRATTERA, physicians should routinely inquire about such possible side effects.

Unless otherwise specified, these adverse reactions have occurred in adults and children and adolescents. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

General disorders and administration site conditions - Lethargy. Musculoskeletal system - Rhabdomyolysis. Nervous system disorders - Hypoaesthesia; paraesthesia in children and adolescents; sensory disturbances; tics. Seizures - Seizures have been reported in the postmarketing period. The postmarketing seizure cases include patients with pre-existing seizure disorders and those with identified risk factors for seizures, straterra and high blood pressure, as well as patients with neither a history of nor identified risk factors for seizures.

Skin and subcutaneous tissue disorders - Alopeciahyperhidrosis. Urogenital system - Male pelvic pain ; urinary hesitation in children and adolescents; urinary retention in children and adolescents. Last reviewed on RxList: Strattera Side Effects Center.

Find Lowest Prices on. Stop using this medicine and call your doctor at once if you have: Common side effects may home built police scanner antenna plans Cardiovascular system - QT prolongation, syncope. Psychiatric disorders - Depression and depressed mood; anxiety, libido changes.

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Straterra and high blood pressure

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