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Acetazolamide adverse events reported to FDA.

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Summary

FDA Adverse Reports: 34. View All

Acetazolamide FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 19

Acetazolamide Dosage, Warnings, Usage.

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Often additional risks of using a medication, such as Acetazolamide, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Acetazolamide users, Learn more about unwanted side effects & find ways to reduce them. Browse Acetazolamide Adverse Reports reported to FDA and participate in Acetazolamide discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Acetazolamide. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Acetazolamide Adverse Effect Reports (FDA)

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6994659-2 | Ataxia, Fall, Gait Disturbance, Mental Status Changes
on Sep 15, 2010 Male patient from UNITED STATES , 61 years of age, weighting 191.8 lb, was diagnosed with hydrocephalus (What is hydrocephalus?) and was treated with Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: ataxia (What is ataxia?), fall (What is fall?), gait disturbance, mental status changes. Acetazolamide dosage: Mg Bid Po. Patient was hospitalized.

6888522-5 | Conjunctival Oedema, Eye Movement Disorder, Eyelid Oedema, Intraocular Pressure Increased
Patient was taking Acetazolamide (View Usage). Patient had the following side effects: conjunctival oedema, eye movement disorder, eyelid oedema, intraocular pressure increased on Jul 19, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 63 years of age, was diagnosed with glaucoma surgery and. Acetazolamide dosage: 8 Ml, Single.

6821805-3 | Abdominal Discomfort, Product Substitution Issue
Adverse event was reported on Jul 07, 2010 by a Female patient taking Acetazolamide (View Usage) (Dosage: 500 Mg Bid Lifetime Need) was diagnosed with benign intracranial hypertension and. Location: UNITED STATES , 56 years of age, weighting 376.0 lb, After Acetazolamide was administered, patient had the following side effects: abdominal discomfort, product substitution issue.

6770598-7 | Ileus Paralytic
on Jun 07, 2010 Male patient from ITALY , 75 years of age, was diagnosed with glaucoma (What is glaucoma?) and was treated with Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: ileus paralytic. Acetazolamide dosage: 125 Mg, Bid. Patient was hospitalized.


6723459-3 | Faecaloma, Ileus Paralytic
on Apr 29, 2010 Male patient from ITALY , 75 years of age, was diagnosed with glaucoma (What is glaucoma?) and was treated with Acetazolamide (View Usage). Patient had the following side effects: faecaloma, ileus paralytic. Acetazolamide dosage: 125 Mg 2x/day, Oral. During the same period patient was treated with AMILORIDE HYDROCHLORIDE (View Amiloride Hydrochloride Review and Amiloride Hydrochloride Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), PREDNISONE (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

6525747-2 | Arrhythmia, Cardiac Failure Chronic, Cardiomyopathy, Cardiopulmonary Failure, Lung Neoplasm Malignant, Pericarditis, Ventricular Arrhythmia
Patient was taking Acetazolamide (View Usage). After Acetazolamide was administered, patient had the following side effects: arrhythmia (What is arrhythmia?), cardiac failure chronic, cardiomyopathy (What is cardiomyopathy?), cardiopulmonary failure, lung neoplasm malignant, pericarditis, ventricular arrhythmia on Dec 09, 2009 from RUSSIAN FEDERATION Additional patient health information: Female patient , 53 years of age, weighting 176.0 lb, was diagnosed with neurological symptom and. Acetazolamide dosage: 250 Mg, 3x/day, Oral. During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), SUNITINIB MALATE (View Sunitinib Malate Review and Sunitinib Malate Label ). Patient was hospitalized.

6391527-4 | Acidosis, Agitation, Cholecystitis, Cholelithiasis, Dyspnoea, Heart Rate Increased, Injection Site Cellulitis, Paraesthesia, Paraesthesia Oral
Adverse event was reported on Sep 17, 2009 by a Male patient taking Acetazolamide (View Usage) (Dosage: 125 Mg, Once, Oral) was diagnosed with mountain sickness acute, prophylaxis and. Location: UNITED STATES , 46 years of age, weighting 180.0 lb, Patient experienced the following unwanted or unexpected effects: acidosis, agitation, cholecystitis, cholelithiasis, dyspnoea, heart rate increased, injection site cellulitis, paraesthesia, paraesthesia oral. During the same period patient was treated with CELEBREX (View Celebrex Review and Celebrex Label ), ADVIL (View Advil Review and Advil Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ).

6379549-0 | Cholelithiasis, Dyspnoea, Heart Rate Increased, Paraesthesia, Swollen Tongue
on Sep 11, 2009 Male patient from UNITED STATES , 46 years of age, weighting 180.0 lb, was diagnosed with mountain sickness acute, prophylaxis and was treated with Acetazolamide (View Usage). Patient had the following side effects: cholelithiasis, dyspnoea, heart rate increased, paraesthesia, swollen tongue. Acetazolamide dosage: 125 Mg, Once, Oral. During the same period patient was treated with CELEBREX (View Celebrex Review and Celebrex Label ), ADVIL (View Advil Review and Advil Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ).

6375192-8 | Asthenia, Blood Chloride Increased, Blood Urea Increased, Confusional State, Decreased Appetite, Depressive Symptom, Lethargy, Metabolic Acidosis, Parkinson's Disease
on Sep 22, 2009 Male patient from UNITED STATES , 67 years of age, was diagnosed with normal pressure hydrocephalus and was treated with Acetazolamide (View Usage). After Acetazolamide was administered, patient had the following side effects: asthenia, blood chloride increased, blood urea increased, confusional state, decreased appetite, depressive symptom, lethargy, metabolic acidosis, parkinson's disease (What is parkinson's disease?). Acetazolamide dosage: 250 Mg Qam Oropharingeal. During the same period patient was treated with MULTIVITAMIN WITH MINERALS (View Multivitamin With Minerals Review and Multivitamin With Minerals Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), DIVALPROEX SODIUM (View Divalproex Sodium Review and Divalproex Sodium Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), DONEPEZIL HCL (View Donepezil Hcl Review and Donepezil Hcl Label ), SERTRALINE HCL (View Sertraline Hcl Review and Sertraline Hcl Label ), CARBIDOPA LEVODOPA (View Carbidopa-levodopa Review and Carbidopa-levodopa Label ).

6328963-8 | Cough, Decreased Appetite, Dizziness, Dysgeusia, Feeling Abnormal, Increased Upper Airway Secretion, Somnolence, Tremor
Patient was taking Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: cough, decreased appetite, dizziness (What is dizziness?), dysgeusia, feeling abnormal, increased upper airway secretion, somnolence, tremor on Aug 24, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 160.0 lb, was diagnosed with mountain sickness acute and. Acetazolamide dosage: 1 Day Before Trip 1 Daily Until Gon Po.

6213789-6 | Burning Sensation, Dysgeusia, Headache, Paraesthesia, Product Substitution Issue, Tooth Disorder, Tooth Fracture, Tooth Hypoplasia, Vomiting
Adverse event was reported on May 21, 2009 by a Female patient taking Acetazolamide (View Usage) (Dosage: 250 Mg, 4 Times Daily, Oral) was diagnosed with benign intracranial hypertension and. Location: UNITED STATES , 31 years of age, Patient had the following side effects: burning sensation, dysgeusia, headache (What is headache?), paraesthesia, product substitution issue, tooth disorder (What is tooth disorder?), tooth fracture, tooth hypoplasia, vomiting.

6110891-4 | Hypokalaemia, Paralysis
on Mar 10, 2009 Male patient from UNITED STATES , 23 years of age, weighting 215.0 lb, was diagnosed with hypokalaemia, paralysis (What is paralysis?) and was treated with Acetazolamide (View Usage). After Acetazolamide was administered, patient had the following side effects: hypokalaemia, paralysis (What is paralysis?). Acetazolamide dosage: 1/2 Tablet Every 6 Hours Po.

6099919-8 | Acidosis, Cough, Dizziness, Dyspnoea, Incorrect Dose Administered, Loss Of Consciousness
on Mar 02, 2009 Male patient from UNITED STATES , child 5 years of age, weighting 40.00 lb, was diagnosed with spinocerebellar ataxia and was treated with Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: acidosis, cough, dizziness (What is dizziness?), dyspnoea, incorrect dose administered, loss of consciousness. Acetazolamide dosage: 1500 Mg Daily Po. Patient was hospitalized.

5965968-0 | Condition Aggravated, Confusional State, Dementia, Urinary Tract Infection
Patient was taking Acetazolamide (View Usage). Patient had the following side effects: condition aggravated, confusional state, dementia (What is dementia?), urinary tract infection (What is urinary tract infection?) on Nov 21, 2008 from UNITED STATES Additional patient health information: Male patient , 82 years of age, weighting 178.4 lb, . Acetazolamide dosage: 500 Mg Bid Po. Patient was hospitalized.

5819689-5 | Ataxia, Condition Aggravated, Dysarthria, Hyperammonaemia, Metabolic Acidosis, Metabolic Encephalopathy, Nystagmus
Adverse event was reported on Jul 10, 2008 by a Male patient taking Acetazolamide (View Usage) (Dosage: 250 Mg Four Times A Day, Oral) was diagnosed with spinocerebellar ataxia and. Location: KOREA, REPUBLIC OF , 49 years of age, After Acetazolamide was administered, patient had the following side effects: ataxia (What is ataxia?), condition aggravated, dysarthria, hyperammonaemia, metabolic acidosis, metabolic encephalopathy, nystagmus.

5778399-3 | Anaemia, Asthenia, Confusional State, Decreased Appetite, Disorientation, Energy Increased, Hypersomnia, Metabolic Acidosis, Paraesthesia
on Jun 18, 2008 Male patient from UNITED STATES , 64 years of age, weighting 155.4 lb, was diagnosed with glaucoma (What is glaucoma?) and was treated with Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, asthenia, confusional state, decreased appetite, disorientation, energy increased, hypersomnia, metabolic acidosis, paraesthesia. Acetazolamide dosage: 250 Mg Qid Po. Patient was hospitalized.

5648853-3 | Acidosis, Azotaemia, Blood Creatinine Increased, Blood Urea Increased, Confusional State, Dehydration, Hyperglycaemia, Mental Status Changes, Renal Tubular Acidosis
on Mar 03, 2008 Male patient from UNITED STATES , 73 years of age, was diagnosed with glaucoma (What is glaucoma?), iris neovascularisation and was treated with Acetazolamide (View Usage). Patient had the following side effects: acidosis, azotaemia, blood creatinine increased, blood urea increased, confusional state, dehydration, hyperglycaemia, mental status changes, renal tubular acidosis. Acetazolamide dosage: 250mg Bid Po. Patient was hospitalized.

5648019-7 | Asthenia, Ataxia, Memory Impairment
Patient was taking Acetazolamide (View Usage). After Acetazolamide was administered, patient had the following side effects: asthenia, ataxia (What is ataxia?), memory impairment on Feb 29, 2008 from UNITED STATES Additional patient health information: Male patient , 81 years of age, . Acetazolamide dosage: 250 Mg Bid Po.

5643773-2 | Ataxia, Condition Aggravated, Hyperammonaemia, Metabolic Acidosis, Upper Respiratory Tract Infection
Adverse event was reported on Feb 15, 2008 by a Male patient taking Acetazolamide (View Usage) (Dosage: 250mg/x4 A Day) was diagnosed with ataxia (What is ataxia?) and. Location: UNITED STATES , 49 years of age, Patient experienced the following unwanted or unexpected effects: ataxia (What is ataxia?), condition aggravated, hyperammonaemia, metabolic acidosis, upper respiratory tract infection.

5591196-7 | Condition Aggravated, Decreased Appetite, Disease Progression, Fatigue, Macular Cyst, Macular Oedema, Paraesthesia, Visual Acuity Reduced, Visual Disturbance
on Jan 07, 2008 Male patient from UNITED STATES , 44 years of age, was diagnosed with macular oedema and was treated with Acetazolamide (View Usage). Patient had the following side effects: condition aggravated, decreased appetite, disease progression, fatigue, macular cyst, macular oedema, paraesthesia, visual acuity reduced, visual disturbance. Acetazolamide dosage: 500mg, Qd, Oral.

5528364-6 | Ammonia Increased, Ataxia, Condition Aggravated, Dizziness, Dysarthria, Hyperammonaemia, Metabolic Acidosis, Nystagmus
on Nov 20, 2007 Male patient from KOREA, REPUBLIC OF , 49 years of age, was diagnosed with ataxia (What is ataxia?) and was treated with Acetazolamide (View Usage). After Acetazolamide was administered, patient had the following side effects: ammonia increased, ataxia (What is ataxia?), condition aggravated, dizziness (What is dizziness?), dysarthria, hyperammonaemia, metabolic acidosis, nystagmus. Acetazolamide dosage: 250mg, Qid, Oral. Patient was hospitalized.

5503967-3 | Confusional State, Fall
Patient was taking Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, fall (What is fall?) on Oct 30, 2007 from UNITED STATES Additional patient health information: Male patient , 75 years of age, was diagnosed with macular oedema, retinal oedema and. Acetazolamide dosage: 500mg Bid Po. Patient was hospitalized.

5500130-7 | Angle Closure Glaucoma, Choroidal Effusion
Adverse event was reported on Oct 18, 2007 by a Male patient taking Acetazolamide (View Usage) (Dosage: 250 Mg, X 2, Oral) . Location: INDIA , 66 years of age, Patient had the following side effects: angle closure glaucoma, choroidal effusion. Patient was hospitalized.

5490476-3 | Blood Electrolytes Abnormal, Hypokalaemia, Hyponatraemia, Metabolic Acidosis
on Oct 17, 2007 Male patient from UNITED STATES , 84 years of age, was treated with Acetazolamide (View Usage). After Acetazolamide was administered, patient had the following side effects: blood electrolytes abnormal, hypokalaemia, hyponatraemia, metabolic acidosis. Acetazolamide dosage: 250mg Qid Po. Patient was hospitalized.

5420833-2 | Renal Failure Acute
on Aug 07, 2007 Male patient from SPAIN , 58 years of age, was diagnosed with maculopathy and was treated with Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure acute. Acetazolamide dosage: 250 Mg, Q8h, Oral. Patient was hospitalized.

5389154-0 | Metabolic Acidosis
Patient was taking Acetazolamide (View Usage). Patient had the following side effects: metabolic acidosis on Jul 13, 2007 from UNITED STATES Additional patient health information: Male patient , 65 years of age, was diagnosed with benign intracranial hypertension and. Acetazolamide dosage: 250mg Bid Po. Patient was hospitalized.

5383839-8 | Renal Failure Acute
Adverse event was reported on Jun 26, 2007 by a Male patient taking Acetazolamide (View Usage) (Dosage: 250 Mg/8h;) was diagnosed with maculopathy and. Location: UNITED STATES , 58 years of age, After Acetazolamide was administered, patient had the following side effects: renal failure acute. Patient was hospitalized.

5094843-1 | Abdominal Pain Upper, Pancreatitis
on Aug 31, 2006 Female patient from UNITED STATES , 17 years of age, weighting 160.0 lb, was treated with Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, pancreatitis. Acetazolamide dosage: 250mg Three Times Daily Po. During the same period patient was treated with ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), CREON (View Creon Review and Creon Label ), TEGASEROD (View Tegaserod Review and Tegaserod Label ), METHADONE HCL (View Methadone Hcl Review and Methadone Hcl Label ), MONTELUKAST (View Montelukast Review and Montelukast Label ), HYDROXYCHLOROQUINE SULFATE (View Hydroxychloroquine Sulfate Review and Hydroxychloroquine Sulfate Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), FEXOFENODINE (View Fexofenodine Review and Fexofenodine Label ).

5088091-9 | Blood Glucose Increased, Metabolic Acidosis
on Aug 23, 2006 Male patient from UNITED STATES , 38 years of age, weighting 161.0 lb, was treated with Acetazolamide (View Usage). Patient had the following side effects: blood glucose increased, metabolic acidosis. Acetazolamide dosage: 250 Mg Qid. Patient was hospitalized.

5069424-6 | Dehydration, Diabetes Mellitus Inadequate Control, Diarrhoea, Renal Failure Acute
Patient was taking Acetazolamide (View Usage). After Acetazolamide was administered, patient had the following side effects: dehydration, diabetes mellitus inadequate control, diarrhoea, renal failure acute on Aug 02, 2006 from UNITED STATES Additional patient health information: Male patient , 55 years of age, weighting 149.9 lb, was diagnosed with glaucoma (What is glaucoma?) and. Acetazolamide dosage: 250 Mg Po Tid. Patient was hospitalized.

4984930-8 | Anaphylactic Reaction, Rash
Adverse event was reported on Feb 24, 2006 by a Male patient taking Acetazolamide (View Usage) (Dosage: ) . Location: UNITED STATES , 65 years of age, Patient experienced the following unwanted or unexpected effects: anaphylactic reaction, rash (What is rash?).

4922102-3 | Confusional State, Dehydration, Electrolyte Imbalance
on Feb 22, 2006 Female patient from UNITED STATES , 82 years of age, weighting 139.0 lb, was diagnosed with glaucoma (What is glaucoma?), pain (What is pain?) and was treated with Acetazolamide (View Usage). Patient had the following side effects: confusional state, dehydration, electrolyte imbalance. Acetazolamide dosage: 500 Mg Bid 3 Days Last Week. During the same period patient was treated with IBUPROFEN (200 Mg Po Prn Occasional) (View Ibuprofen Review and Ibuprofen Label ), NORVASC (View Norvasc Review and Norvasc Label ), DIOVAN (View Diovan Review and Diovan Label ), XANAX (View Xanax Review and Xanax Label ), NOMENDA (View Nomenda Review and Nomenda Label ), EFFEXOR (View Effexor Review and Effexor Label ), COSOPT (View Cosopt Review and Cosopt Label ), LOTEMAX (View Lotemax Review and Lotemax Label ). Patient was hospitalized.

4883287-0 | Confusional State, Disorientation
on Jan 17, 2006 Male patient from UNITED STATES , weighting 185.2 lb, was treated with Acetazolamide (View Usage). After Acetazolamide was administered, patient had the following side effects: confusional state, disorientation. Acetazolamide dosage: 500mg Bid Po. Patient was hospitalized.

4674930-X | Transient Ischaemic Attack
Patient was taking Acetazolamide (View Usage). Patient experienced the following unwanted or unexpected effects: transient ischaemic attack on May 10, 2005 from Additional patient health information: Female patient , 62 years of age, was diagnosed with vertebral artery occlusion and. Acetazolamide dosage: 1000mg.


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Acetazolamide Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

Jennifer martinez   Makati City

7:40am on Sunday, October 25th, 2009

My mom took 9 tablets of the acetazolamide until the doctor advised her to stop taking it due to dis... read more »

To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Acetazolamide risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Acetazolamide quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Acetazolamide use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Acetazolamide Reactions
Abdominal Discomfort
Abdominal Pain Upper
Acidosis
Agitation
Ammonia Increased
Asthenia
AtaxiaWhat is Ataxia?
Blood Urea Increased
Cholelithiasis
Condition Aggravated
Confusional State
Cough
Decreased Appetite
Dehydration
Disorientation
DizzinessWhat is Dizziness?
Dysarthria
Dysgeusia
Dyspnoea
FallWhat is Fall?
Heart Rate Increased
Hyperammonaemia
Hypokalaemia
Ileus Paralytic
Mental Status Changes
Metabolic Acidosis
Nystagmus
Paraesthesia
Product Substitution Issue
Renal Failure Acute
Acetazolamide Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Acetazolamide adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!