"Oct. 24, 2012 -- Women who take hormones within five years of menopause may have a slightly lower risk of Alzheimer's disease compared to women who don't ever take them, a new study shows.
The study, which is published in the journal Ne"...
Cognex Side Effects Center
Medical Editor: John P. Cunha, DO, FACOEP
Cognex (tacrine hydrochloride) is used to treat patients with Alzheimer's disease or mild to moderate dementia. Cognex is discontinued in the U.S., but generic versions may be available. Common side effects include nausea, stomach upset, vomiting, diarrhea, shaking, and skin rash.
The recommended dosage is 19 to 20 mg four times daily, or as directed by your doctor. Cognex may interact with aspirin, atropine, cimetidine, dicyclomine, donepezil, fluvoxamine, galantamine, glycopyrrolate, hyoscyamine, mepenzolate, methscopolamine, NSAIDs, propantheline, rivastigmine, scopolamine, or theophylline. Tell your doctor all medications and supplements you take. It is not known if Cognex causes fetal harm when taken by a pregnant woman or whether it passes into breast milk. Consult your doctor before taking Cognex if you are pregnant or before breastfeeding.
Our Cognex (tacrine hydrochloride) Side Effects Center provides a comprehensive view of available drug information on the potential side effects 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. You may report side effects to FDA at 1-800-FDA-1088.
What is Patient Information in Detail?
Easy-to-read and understand detailed drug information and pill images for the patient or caregiver from Cerner Multum.
Cognex in Detail - Patient Information: Side Effects
Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Call your doctor at once if you have any of these serious side effects:
- confusion, hallucinations;
- extreme or sudden changes in behavior;
- seizure (convulsions);
- pain or burning when you urinate; or
- nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes).
Less serious side effects of tacrine include:
- mild nausea, vomiting, diarrhea, upset stomach;
- weight loss;
- urinating more than usual;
- agitation, depressed mood;
- skin rash, increased sweating;
- fever or chills, runny nose, cough;
- dizziness, drowsiness, tired feeling;
- joint or muscle pain; or
- weakness, lack of coordination.
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.
Read the entire detailed patient monograph for Cognex (Tacrine) »
What is Prescribing information?
The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.
Cognex FDA Prescribing Information: Side Effects
Common Adverse Events Leading to Discontinuation
In clinical trials, approximately 17% of the 2706 patients who received Cognex® (tacrine) and 5% of the 1886 patients who received placebo withdrew permanently because of adverse events. It should be noted that some of the placebo-treated patients were exposed to Cognex® (tacrine) prior to receiving placebo due to the variety of study designs used, including crossover studies. Transaminase elevations were the most common reason for withdrawals during Cognex® (tacrine) treatment (8% of all Cognex® (tacrine) -treated patients, or 212 of 456 patients withdrawn). The controlled clinical trial protocols required that any patient with an ALT/SGPT elevation > 3 X ULN be withdrawn, because of concern about potential hepatotoxicity. Apart from withdrawals due to transaminase elevations, 244 patients (9%) withdrew for adverse events while receiving Cognex® (tacrine) .
Other adverse events that most frequently led to the withdrawal of tacrine-treated patients in clinical trials were nausea and/or vomiting (1.5%), agitation (0.9%), rash (0.7%), anorexia (0.7%), and confusion (0.5%). These adverse events also most frequently led to the withdrawal of placebo-treated patients, although at lower frequencies (0.1% to 0.2%).
Most Frequent Adverse Clinical Events Seen in Association With the Use of Tacrine
The events identified here are those that occurred at an absolute incidence of at least 5% of patients treated with Cognex® (tacrine) , and at a rate at least 2-fold higher in patients reated with Cognex (tacrine) ®than placebo.
The most common adverse events associated with the use of Cognex® (tacrine) were elevated transaminases, nausea and/or vomiting, diarrhea, dyspepsia, myalgia, anorexia, and ataxia. Of these events, nausea and/or vomiting, diarrhea, dyspepsia, and anorexia appeared to be dose-dependent.
Adverse Events Reported in Controlled Trials
The events cited in the tables below reflect experience gained under closely monitored conditions of clinical trials with a highly selected patient population. In actual clinical practice or in other clinical trials, these frequency estimates may not apply, as the conditions of use, reporting behavior, and the kinds of patients treated may differ.
Table 3 lists treatment-emergent signs and symptoms that occurred in at least 2% of patients with Alzheimer's disease in placebo-controlled trials and who received the recommended regimen for dose introduction and titration of Cognex® (see DOSAGE AND ADMINISTRATION).
Table 3. Adverse Events Occurring in at Least 2% of Patients
Receiving Cognex® (tacrine) at a Starting Dose of 40 mg/day with Titration in 40 mg/day
Increments Every 6 Weeks in Controlled Clinical Trials [Number (%) of Patients]
N = 634
N = 342
|Elevated Transaminasea||184 (29)||5 (2)|
|BODY AS A WHOLE|
|Headache||67 (11)||52 (15)|
|Fatigue||26 (4)||9 (3)|
|Chest Pain||24 (4)||18 (5)|
|Weight Decrease||21 (3)||4 (1)|
|Back Pain||15 (2)||14 (4)|
|Asthenia||15 (2)||7 (2)|
|Nausea and/or Vomiting||178 (28)||29 (9)|
|Diarrhea||99 (16)||18 (5)|
|Dyspepsia||57 (9)||22 (6)|
|Anorexia||54 (9)||11 (3)|
|Abdominal Pain||48 (8)||24 (7)|
|Flatulence||22 (4)||5 (2)|
|Constipation||24 (4)||8 (2)|
|HEMIC AND LYMPHATIC SYSTEM|
|Purpura||15 (2)||8 (2)|
|Myalgia||54 (9)||18 (5)|
|Dizziness||73 (12)||39 (11)|
|Confusion||42 (7)||24 (7)|
|Ataxia||36 (6)||12 (4)|
|Insomnia||37 (6)||18 (5)|
|Somnolence||22 (4)||11 (3)|
|Tremor||14 (2)||2 (<1)|
|Agitation||43 (7)||30 (9)|
|Depression||22 (4)||14 (4)|
|Thinking Abnormal||17 (3)||14 (4)|
|Anxiety||16 (3)||7 (2)|
|Hallucination||15 (2)||12 (4)|
|Hostility||15 (2)||5 (2)|
|Rhinitis||51 (8)||22 (6)|
|Upper Respiratory Infection||18 (3)||11 (3)|
|Coughing||17 (3)||18 (5)|
|SKIN AND APPENDAGES|
|Rashb||46 (7)||18 (5)|
|Facial Flushing, Skin Flushing||16 (3)||3 (<1)|
|Urination Frequency||21 (3)||12 (4)|
|Urinary Tract Infection||21 (3)||20 (6)|
|Urinary Incontinence||16 (3)||9 (3)|
|aALT or AST value of approximately 3 X ULN or greater
orthat resulted in a change in patient management. Patients were monitored
bIncludes COSTART terms: rash, rash-erythematous,rash-maculopapular, urticaria, petechialrash, rash-vesiculobullous, and pruritus.
Other Adverse Events Observed During All Clinical Trials
Cognex® (tacrine) has been administered to 2706 individuals during clinical trials.A total of 1471 patients were treated for at least 3 months, 1137 for at least 6 months, and 773 for at least 1 year. Any untoward reactions that occurred during these trials were recorded as adverse events by the clinical investigators using terminology of their own choosing. To provide a meaningful estimate of the proportion of individuals having similar types of events, the events were grouped into a smaller number of standardized categories using a modified COSTART dictionary. These categories are used in the listing below. The frequencies represent the proportion of the 2706 individuals exposed to Cognex® (tacrine) who experienced that event while receiving Cognex (tacrine) ®. All adverse events are included except those already listed on the previous table and those COSTART terms too general to be informative. Events are further classified by body system categories and listed using the following definitions: frequent adverse events are defined as those occurring in at least 1/100 patients; infrequent adverse events are those occurring in 1/100 to 1/1000 patients; and rare adverse events are those occurring in less than 1/1000 patients. These adverse events are not necessarily related to Cognex® (tacrine) treatment. Only rare adverse events deemed to be potentially important are included.
Body As a Whole: Frequent: Chill, fever, malaise, peripheral edema. Infrequent: Face edema, dehydration, weight increase, cachexia, edema (generalized), lipoma. Rare: Heat exhaustion, sepsis, cholingeric crisis, death.
Cardiovascular System: Frequent: Hypotension, hypertension. Infrequent: Heart failure, myocardial infarction, angina pectoris, cerebrovascular accident, transient schemic attack, phlebitis, venous insufficiency, abdominal aortic aneurysm, atrial fibrillation or flutter, palpitation, tachycardia, bradycardia, pulmonary embolus, migraine, hypercholesterolemia. Rare: Heart arrest, premature atrial contractions, A-V block, bundle branch block.
Digestive System: Infrequent: Glossitis, gingivitis, mouth or throat dry, stomatitis, increased salivation, dysphagia, esophagitis, gastritis, gastroenteritis, GI hemorrhage, stomach ulcer, hiatal hernia, hemorrhoids, stools bloody, diverticulitis, fecal impaction, fecal incontinence, hemorrhage (rectum), cholelithiasis, cholecystitis, increased appetite. Rare: Duodenal ulcer, bowel obstruction.
Nervous System: Frequent: Convulsions, vertigo, syncope, hyperkinesia, paresthesia. Infrequent: Dreaming abnormal, dysarthria, aphasia, amnesia, wandering, twitching, hypesthesia, delirium, paralysis, bradykinesia, movement disorder, cogwheel rigidity, paresis, neuritis, hemiplegia, Parkinson's disease, neuropathy, extrapyramidal syndrome, reflexes decreased/absent. Rare: Tardive dyskinesia, dysesthesia, dystonia, encephalitis, coma, apraxia, oculogyric crisis, akathisia, oral facial dyskinesia, Bell's palsy, exacerbation of Parkinson 's disease.
Respiratory System: Frequent: Pharyngitis, sinusitis, bronchitis, pneumonia, dyspnea. Infrequent: Epistaxis, chest congestion, asthma, hyperventilation, lower respiratory infection. Rare: Hemoptysis, lung edema, lung cancer, acute epiglottitis.
Skin and Appendages: Frequent: Sweating increased. Infrequent: Acne, alopecia, dermatitis, eczema, skin dry, herpes zoster, psoriasis, cellulitis, cyst, furunculosis, herpes simplex, hyperkeratosis, basal cell carcinoma, skin cancer. Rare: Desquamation, seborrhea, squamous cell carcinoma, ulcer (skin), skin necrosis, melanoma.
Urogenital System: Infrequent: Hematuria, renal stone, kidney infection, glycosuria, dysuria, polyuria, nocturia, pyuria, cystitis, urinary retention, urination urgency, vaginal hemorrhage, pruritus (genital), breast pain, impotence, prostate cancer. Rare: Bladder tumor, renal tumor, renal failure, urinary obstruction, breast cancer, epididymitis, carcinoma (ovary).
Special Senses: Frequent: Conjunctivitis. Infrequent: Cataract, eyes dry, eye pain, visual field defect, diplopia, amblyopia, glaucoma, hordeolum, deafness, earache, tinnitus, inner ear infection, otitis media, unusual taste. Rare: Vision loss, ptosis, blepharitis, labyrinthitis, inner ear disturbance.
Voluntary reports of adverse events temporally associated with Cognex® (tacrine) that have been received since market introduction, that are not listed above, and that may have no causal relationship with the drug include the following: pancreatitis, perforated peptic ulcer, and falling.
Read the entire FDA prescribing information for Cognex (Tacrine) »
Additional Cognex Information
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