QMIIZ ODT

QMIIZ ODT- meloxicam tablet, orally disintegrating
TerSera Therapeutics LLC

WARNING: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS

See full prescribing information for complete boxed warning.

  • Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use [ see Warning and Precautions (5.1) ]
  • QMIIZ ODT is contraindicated in the setting of coronary artery bypass graft (CABG) surgery [ see Contradictions (4), Warnings and Precautions (5.1) ]
  • NSAIDs cause an increased risk of serious gastrointestinal (GI) adverse events including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal. These events can occur at any time during use and without warning symptoms. Elderly patients and patients with a prior history of peptic ulcer disease and/or GI bleeding are at greater risk for serious GI events ( see Warnings and Precautions (5.2)].

1 INDICATIONS AND USAGE

1.1 Osteoarthritis (OA)

QMIIZ ODT is indicated for relief of the signs and symptoms of osteoarthritis in adults [see Clinical Studies (14.1) ].

1.2 Rheumatoid Arthritis (RA)

QMIIZ ODT is indicated for relief of the signs and symptoms of rheumatoid arthritis in adults [see Clinical Studies (14.1) ].

1.3 Juvenile Rheumatoid Arthritis (JRA) Pauciarticular and Polyarticular Course

QMIIZ ODT is indicated for relief of the signs and symptoms of pauciarticular or polyarticular course juvenile rheumatoid arthritis in pediatric patients who weigh greater than or equal to 60 kg [see Dosage and Administration (2.4) and Clinical Studies (14.2)].

2 DOSAGE AND ADMINISTRATION

2.1 General Dosing Instructions

Carefully consider the potential benefits and risks of QMIIZ ODT and other treatment options before deciding to use QMIIZ ODT. Use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals [see Warnings and Precautions (5) ].

After observing the response to initial therapy with QMIIZ ODT, adjust the dose to suit an individual patient’s needs.

In adults, the maximum recommended daily oral dose of QMIIZ ODT is 15 mg regardless of formulation. In patients with hemodialysis, a maximum daily dosage of 7.5 mg is recommended [see Use in Specific Populations (8.7) and Clinical Pharmacology (12.3)].

With QMIIZ ODT, administration with liquid is not necessary. QMIIZ ODT may be taken without regard to timing of meals.

QMIIZ ODT should be taken as follows:

  • Leave QMIIZ ODT in the original package until the time of administration.
  • Be sure that hands are dry when handling an orally disintegrating tablet.
  • Open the carton and peel back the foil on the blister. Do not push the tablet through the foil as this could damage the tablet.
  • Gently remove the tablet from the blister and place it in the mouth, or onto the tongue, immediately after removing from the blister.
  • The tablet will disintegrate quickly in saliva and can be easily swallowed with or without drinking liquid.

2.2 Osteoarthritis

For the relief of the signs and symptoms of osteoarthritis, the recommended starting and maintenance oral dose of QMIIZ ODT is 7.5 mg once daily. Some patients may receive additional benefit by increasing the dose to 15 mg once daily.

2.3 Rheumatoid Arthritis

For the relief of the signs and symptoms of rheumatoid arthritis, the recommended starting and maintenance oral dose of QMIIZ ODT is 7.5 mg once daily. Some patients may receive additional benefit by increasing the dose to 15 mg once daily.

2.4 Juvenile Rheumatoid Arthritis (JRA) Pauciarticular and Polyarticular Course

For the treatment of juvenile rheumatoid arthritis, the recommended oral dose of QMIIZ ODT is 7.5 mg once daily in children who weigh greater than or equal to 60 kg. There was no additional benefit demonstrated by increasing the dose above 7.5 mg in clinical trials.

Only use QMIIZ ODT tablets in children who weigh greater than or equal to 60 kg.

2.5 Renal Impairment

The use of QMIIZ ODT in subjects with severe renal impairment is not recommended.

In patients on hemodialysis, the maximum dosage of QMIIZ ODT is 7.5 mg per day [see Use in Specific Populations (8.7) and Clinical Pharmacology (12.3)].

2.6 Non-Interchangeability with Other Formulations of Meloxicam

QMIIZ ODT (meloxicam) orally disintegrating tablets have not shown equivalent systemic exposure with a comparable pharmacokinetic profile to other approved formulations of oral meloxicam. Therefore, QMIIZ ODT tablets are not interchangeable with other formulations of oral meloxicam product even if the total milligram strength is the same. Do not substitute similar dose strengths of QMIIZ ODT with other formulations of oral meloxicam products.

3 DOSAGE FORMS AND STRENGTHS

QMIIZ ODT (meloxicam) orally disintegrating tablet is a freeze-dried orally administered formulation containing 7.5 mg or 15 mg meloxicam and is designed to rapidly disintegrate in the mouth. Both strengths are orange-flavored, yellow, circular tablets and are debossed with an identifying marking: either 7.5 or 15 (see images below).

7.5mg dose 15mg dose
Figure
Figure

4 CONTRAINDICATIONS

QMIIZ ODT is contraindicated in the following patients:

  • Known hypersensitivity (e.g., anaphylactic reactions and serious skin reactions) to meloxicam or any components of the drug product [see Warnings and Precautions (5.7, 5.9)]
  • History of asthma, urticaria, or other allergic-type reactions after taking aspirin or other NSAIDs. Severe, sometimes fatal, anaphylactic reactions to NSAIDs have been reported in such patients [see Warnings and Precautions (5.7, 5.8)]
  • In the setting of coronary artery bypass graft (CABG) surgery [see Warnings and Precautions (5.1) ]
  • Patients with phenylketonuria [see Warnings and Precautions (5.14)]

5 WARNINGS AND PRECAUTIONS

5.1 Cardiovascular Thrombotic Events

Clinical trials of several cyclooxygenase-2 (COX-2) selective and nonselective NSAIDs of up to three years duration have shown an increased risk of serious cardiovascular (CV) thrombotic events, including myocardial infarction (MI) and stroke, which can be fatal. Based on available data, it is unclear that the risk for CV thrombotic events is similar for all NSAIDs. The relative increase in serious CV thrombotic events over baseline conferred by NSAID use appears to be similar in those with and without known CV disease or risk factors for CV disease. However, patients with known CV disease or risk factors had a higher absolute incidence of excess serious CV thrombotic events, due to their increased baseline rate. Some observational studies found that this increased risk of serious CV thrombotic events began as early as the first weeks of treatment. The increase in CV thrombotic risk has been observed most consistently at higher doses.

To minimize the potential risk for an adverse CV event in NSAID-treated patients, use the lowest effective dose for the shortest duration possible. Physicians and patients should remain alert for the development of such events, throughout the entire treatment course, even in the absence of previous CV symptoms. Patients should be informed about the symptoms of serious CV events and the steps to take if they occur.

There is no consistent evidence that concurrent use of aspirin mitigates the increased risk of serious CV thrombotic events associated with NSAID use. The concurrent use of aspirin and an NSAID, such as meloxicam, increases the risk of serious gastrointestinal (GI) events [see Warnings and Precautions (5.2) ].

Status Post-Coronary Artery Bypass Graft (CABG) Surgery

Two large, controlled clinical trials of a COX-2 selective NSAID for the treatment of pain in the first 10-14 days following CABG surgery found an increased incidence of myocardial infarction and stroke. NSAIDs are contraindicated in the setting of CABG [see Contraindications (4) ].

Post-MI Patients

Observational studies conducted in the Danish National Registry have demonstrated that patients treated with NSAIDs in the post-MI period were at increased risk of reinfarction, CV-related death, and all-cause mortality beginning in the first week of treatment. In this same cohort, the incidence of death in the first year post-MI was 20 per 100 person years in NSAID-treated patients compared to 12 per 100 person years in non-NSAID exposed patients. Although the absolute rate of death declined somewhat after the first year post-MI, the increased relative risk of death in NSAID users persisted over at least the next four years of follow-up.

Avoid the use of QMIIZ ODT in patients with a recent MI unless the benefits are expected to outweigh the risk of recurrent CV thrombotic events. If QMIIZ ODT is used in patients with a recent MI, monitor patients for signs of cardiac ischemia.

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