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The uses of Ativan vs. Xanax differ. Doctors will give them to patients with different disorders. They have been FDA approved for patients of different ages as well. Ativan can be used for patients 12 and over while Xanax isn’t prescribed to patients that are under 18.

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Ativan uses:

Ativan dosages are used for patients with anxiety. They can also be used as a preoperative sedative. Ativan is available in a pill or liquid form. The doses are available in 0.5 mg, 1 mg, and 2 mg.

Xanax uses:

Xanax is also given to patients with anxiety. They can additionally help patients who suffer from panic disorder. Xanax is prescribed to adults that are over 18. Xanax comes in Pill, Extended-release, Dissolving tablet, and Liquid form. The doses are available in .25 mg, 0.5 mg, 1 mg, and 2 mg.

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Ativan Off-Label Uses

Off-label Ativan use refers to the drug being prescribed for something different than its FDA approved for. Doctors may choose to prescribe it for purposes that have been proven to work but isn’t an approved use. Here’s what Ativan might be prescribed for:

  • For a patient who is irritable.
  • For someone suffering from mania.
  • Someone who experiences recurring seizures.
  • Pre-surgery sedating.
  • Vomiting due to chemotherapy.
  • Subduing severe seizures.
  • Assisting in alcohol withdrawal to prevent delirium tremens.

Xanax Off-Label Uses

Xanax also has some off-label uses. They include:

  • Relief of irritable bowel syndrome.
  • Someone who experiences premenstrual syndrome.
  • Relief of ringing ears.
  • Prevention of tremors.

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1. WHAT DECA‑DURABOLIN IS AND WHAT IT
IS USED FOR
Deca‑Durabolin is a clear yellow oily solution
for injection containing 50 mg/ml of the active
ingredient nandrolone decanoate.
The active substance, nandrolone decanoate
belongs to the group of medicines known as
anabolic steroids that help to prevent bone loss.
Deca‑Durabolin is used in osteoporosis, when
bones thin and become brittle, after the
menopause.

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2. WHAT YOU NEED TO KNOW BEFORE
DECA‑DURABOLIN IS GIVEN TO YOU
Do not receive Deca‑Durabolin:
• If you are pregnant or think you may be
pregnant (see section 2 “pregnancy, breast-
feeding and fertility”).
• If you are allergic (hypersensitive) to
nandrolone decanoate or any of the
ingredients of this medicine (listed in section
6 “What Deca‑Durabolin contains”).
• In children under the age of 3 years.
• If you have porphyria (an inherited
blood disorder)
If you are allergic to peanuts or soya (see
section 2 “Important information about some of
the ingredients of Deca‑Durabolin”).
Take special care with Deca‑Durabolin:
If you notice any signs of masculinization (for
instance lowering of the voice or increase
in body or facial hair), consult your doctor
immediately.

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Extra supervision by your doctor may be
necessary in some cases; particularly the
elderly. At regular intervals, blood tests will be
done to check the oxygen-carrying substance in
your red blood cells (haemoglobin). In very rare
cases the number of red blood cells will increase
too much leading to complications.
Medical checks may also be necessary in some
other conditions.

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Therapeutic indications

For use in osteoporosis in post-menopausal women.

Established osteoporosis should have been diagnosed by the following parameters:

i) crush or wedge fractures of the vertebrae

ii) other osteoporotic fractures

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iii) established reduction in bone mineral content as measured by accepted BMC measurements.

Posology:

Post-menopausal women

50mg every three weeks

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The duration of treatment depends on the clinical response and the possible occurrence of side-effects.

We would recommend that the effectiveness of therapy be monitored with the appropriate methods for osteoporosis on a 6-12 monthly basis.

Method of administration:

Deca-Durabolin should be administered by deep intramuscular injection

Pregnancy (see section 4.6).

Breast-feeding

Porphyria

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Hypersensitivity to the active substance or to any of the excipients, including arachis oil. Deca-Durabolin is therefore contraindicated in patients allergic to peanuts or soya (see section 4.4).

Medical examination:

Physicians should consider monitoring patients receiving Deca-Durabolin before the start of treatment, at quarterly intervals for the first 12 months and yearly thereafter for the following parameters:

• Hematocrit and hemoglobin to exclude polycythemia.

Conditions that need supervision:

Patients, especially the elderly, with the following conditions should be monitored for:

• Tumours – Mammary carcinoma, hypernephroma, bronchial carcinoma and skeletal metastases. In these patients hypercalcaemia or hypercalciuria may develop spontaneously, and also during androgen therapy. Nevertheless, the hypercalcaemia or hypercalciuria should first be treated appropriately and after restoration of normal calcium levels, if judged necessary and taking into account the risks and benefits on a case by case basis, hormone therapy can be resumed, with caution.

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• Pre-existing conditions-In patients with pre-existing cardiac, renal or hepatic insufficiency/disease or epilepsy or migraine anabolic steroid treatment may cause complications characterized by oedema with or without congestive heart failure. In such cases treatment must be stopped immediately. Patients who experienced myocardial infarction, cardiac-, hepatic- or renal insufficiency, hypertension, epilepsy, or migraine should be monitored due to the risk of deterioration of or reoccurrence of disease. In such cases treatment must be stopped immediately.

• Diabetes mellitus – Deca-Durabolin can improve glucose tolerance in diabetic patients (see section 4.5).

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• Anti-coagulant therapy – Deca-Durabolin can enhance the anti-coagulant action of coumarin-type agents (see also section 4.5).

• Liver dysfunction – caution should be used in patients with severe hepatic impairment and Deca-Durabolin 50mg/ml should only be used if the benefits outweigh the risks.

Adverse events:

If anabolic steroid-associated adverse reactions occur (see section 4.8), treatment with Deca-Durabolin should be discontinued and, upon resolution of complaints, treatment can be resumed.

Virilisation:

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Patients should be informed about the potential occurrence of signs of virilisation. In particular, singers and women with speech professions should be informed about the risk of deepening of the voice.

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