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Summary

FDA Adverse Reports: 121. View All

Lialda FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 61

Lialda Dosage, Warnings, Usage.

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Often additional risks of using a medication, such as Lialda, 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 Lialda users, Learn more about unwanted side effects & find ways to reduce them. Browse Lialda Adverse Reports reported to FDA and participate in Lialda discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Lialda. 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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Lialda Adverse Effect Reports (FDA)

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6211953-3 | Leukopenia
on May 19, 2009 Female patient from UNITED STATES , 26 years of age, weighting 132.1 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: leukopenia. Lialda dosage: 2.4 G, 1x/day:qd, Oral; 3.6, 1x/day:qd, Oral. During the same period patient was treated with CANASA (MESALAZINE) (View Canasa (mesalazine) Review and Canasa (mesalazine) Label ).

6189360-1 | Dyspnoea Exertional, Influenza Like Illness, Sinus Tachycardia, Viral Myocarditis
Patient was taking Lialda (View Usage). Patient had the following side effects: dyspnoea exertional, influenza like illness, sinus tachycardia, viral myocarditis on Apr 28, 2009 from UNITED STATES Additional patient health information: Male patient , 43 years of age, weighting 265.0 lb, was diagnosed with colitis ulcerative and. Lialda dosage: 4.8 G, 1x/day, Oral. During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ), QUESTRAN LIGHT (COLESTYRAMINE) (View Questran Light (colestyramine) Review and Questran Light (colestyramine) Label ). Patient was hospitalized.

6184429-X | Pericarditis
Adverse event was reported on May 07, 2009 by a Female patient taking Lialda (View Usage) (Dosage: 1 Daily) . Location: UNITED STATES , 68 years of age, weighting 160.0 lb, After Lialda was administered, patient had the following side effects: pericarditis. Patient was hospitalized.

6181945-1 | Dehydration, Diarrhoea, Electrolyte Imbalance, Paraesthesia, Pyrexia, White Blood Cell Count Increased
on Apr 27, 2009 Female patient from UNITED STATES , 32 years of age, weighting 89.07 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: dehydration, diarrhoea, electrolyte imbalance, paraesthesia, pyrexia, white blood cell count increased. Lialda dosage: 2.4 G, 1x/day:qd, Oral ; 4.8 G, 1/xday:qd, Oral. Patient was hospitalized.


6181944-X | Duodenal Ulcer Haemorrhage
on Apr 28, 2009 Male patient from UNITED STATES , 18 years of age, weighting 149.9 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient had the following side effects: duodenal ulcer haemorrhage. Lialda dosage: 1.2 G, 2x/day: Bid, Oral. During the same period patient was treated with ROWASA (View Rowasa Review and Rowasa Label ). Patient was hospitalized.

6164446-6 | Cartilage Atrophy, Hypoaesthesia, Spinal Cord Compression
Patient was taking Lialda (View Usage). After Lialda was administered, patient had the following side effects: cartilage atrophy, hypoaesthesia, spinal cord compression on Apr 09, 2009 from UNITED STATES Additional patient health information: Female patient , 53 years of age, weighting 151.9 lb, was diagnosed with colitis and. Lialda dosage: 1.2 G To 2.4 G Daily, Oral. During the same period patient was treated with BENICAR HCT (View Benicar Hct Review and Benicar Hct Label ), NEXIUM (View Nexium Review and Nexium Label ), CLIDINIUM (CLIDINIUM) (View Clidinium (clidinium) Review and Clidinium (clidinium) Label ).

6163698-6 | Abdominal Pain Upper, Alanine Aminotransferase Increased, Pyrexia
Adverse event was reported on Feb 12, 2009 by a Male patient taking Lialda (View Usage) (Dosage: 2.4 G Daily, Oral) was diagnosed with colitis ulcerative and. Location: UNITED STATES , 19 years of age, weighting 158.1 lb, Patient experienced the following unwanted or unexpected effects: abdominal pain upper, alanine aminotransferase increased, pyrexia.

6163696-2 | Myalgia, Pain In Extremity, Pyrexia
on Mar 17, 2009 Female patient from UNITED STATES , 38 years of age, weighting 101.0 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient had the following side effects: myalgia, pain in extremity, pyrexia. Lialda dosage: 2.4 G, 1x/day:qd, Oral : 2.4 G, One Dose, Oral. During the same period patient was treated with ROWASA (View Rowasa Review and Rowasa Label ).

6163691-3 | Pancreatitis
on Mar 24, 2009 Male patient from UNITED STATES , 79 years of age, weighting 220.9 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). After Lialda was administered, patient had the following side effects: pancreatitis. Lialda dosage: 4.8 G, 1x/day:qd, Oral. During the same period patient was treated with UROCIT K (View Urocit-k Review and Urocit-k Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), COLAZAL (View Colazal Review and Colazal Label ), PROAMATINE (View Proamatine Review and Proamatine Label ), TYLENOL ARTHRITIS (PARACETAMOL) (View Tylenol Arthritis (paracetamol) Review and Tylenol Arthritis (paracetamol) Label ). Patient was hospitalized.

6163687-1 | Colitis Ulcerative, Depression
Patient was taking Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: colitis ulcerative, depression (What is depression?) on Oct 24, 2008 from UNITED STATES Additional patient health information: Male patient , 16 years of age, weighting 274.9 lb, was diagnosed with colitis ulcerative and. Lialda dosage: 4.8 G, 1x/day:qd, Oral. Patient was hospitalized.

6163653-6 | Off Label Use, Pancreatitis
Adverse event was reported on Oct 27, 2008 by a Male patient taking Lialda (View Usage) (Dosage: Df, 1x/day:qd, Oral) was diagnosed with crohn's disease (What is crohn's disease?) and. Location: UNITED STATES , 25 years of age, weighting 170.0 lb, Patient had the following side effects: off label use, pancreatitis. During the same period patient was treated with BUDESONIDE (View Budesonide Review and Budesonide Label ), FERROSOL (FERROUS SULFATE) (View Ferrosol (ferrous Sulfate) Review and Ferrosol (ferrous Sulfate) Label ). Patient was hospitalized.

6163652-4 | Rash Erythematous
on Dec 02, 2008 Male patient from UNITED STATES , 80 years of age, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). After Lialda was administered, patient had the following side effects: rash erythematous. Lialda dosage: 4.8 G, 1x/day:qd, Oral. During the same period patient was treated with TRICOR (View Tricor Review and Tricor Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), MULTIVITAMIN (ASCORBIC ACID, CALCIUM PANTOTHENATE, ERGOCALCIFEROL, NIC (View Multivitamin (ascorbic Acid, Calcium Pantothenate, Ergocalciferol, Nic Review and Multivitamin (ascorbic Acid, Calcium Pantothenate, Ergocalciferol, Nic Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), VYTORIN (View Vytorin Review and Vytorin Label ). Patient was hospitalized and became disabled.

6163621-4 | Anxiety, Diarrhoea Haemorrhagic, Pallor
on Aug 04, 2008 Female patient from UNITED STATES , 52 years of age, weighting 117.9 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), diarrhoea haemorrhagic, pallor. Lialda dosage: 1.2 G, 1x/day:qd, Oral : 2.4 G, 1x/day:qd, Oral.

6163593-2 | Flatulence, Haematochezia
Patient was taking Lialda (View Usage). Patient had the following side effects: flatulence, haematochezia on Jun 10, 2008 from UNITED STATES Additional patient health information: Male patient , 68 years of age, weighting 190.0 lb, was diagnosed with irritable bowel syndrome (What is irritable bowel syndrome?) and. Lialda dosage: 2.4 G, 1x/day:qd, Oral. During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), TENORMIN (View Tenormin Review and Tenormin Label ), VYTORIN (View Vytorin Review and Vytorin Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LANTUS (View Lantus Review and Lantus Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), PRANDIN (View Prandin Review and Prandin Label ), AMARYL (View Amaryl Review and Amaryl Label ).

6163494-X | Pancreatitis Acute
Adverse event was reported on Mar 20, 2008 by a Male patient taking Lialda (View Usage) (Dosage: 1.2 G, 2x/day:bid, Oral) was diagnosed with colitis and. Location: UNITED STATES , 34 years of age, After Lialda was administered, patient had the following side effects: pancreatitis acute.

6163490-2 | Pancreatitis
on Feb 11, 2008 Female patient from UNITED STATES , 18 years of age, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: pancreatitis. Lialda dosage: 2.4 G, 1x/day:qd, Oral.

6163481-1 | Pancreatitis
on May 08, 2008 Male patient from UNITED STATES , 37 years of age, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient had the following side effects: pancreatitis. Lialda dosage: 2.4 G, 1x/day:qd, Oral. During the same period patient was treated with ZYRTEC (View Zyrtec Review and Zyrtec Label ). Patient was hospitalized.

6163480-X | Pancreatitis
Patient was taking Lialda (View Usage). After Lialda was administered, patient had the following side effects: pancreatitis on Dec 20, 2007 from UNITED STATES Additional patient health information: Female patient , 16 years of age, was diagnosed with colitis and. Lialda dosage: 4.8 G, 1x/day:qd, Oral. During the same period patient was treated with PREDNISONE (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

6148222-6 | Angioedema, Peripheral Motor Neuropathy
Adverse event was reported on Mar 30, 2009 by a Female patient taking Lialda (View Usage) (Dosage: 2.4 G, 1x/day:qd, Oral) was diagnosed with colitis ulcerative and. Location: UNITED STATES , 67 years of age, weighting 149.9 lb, Patient experienced the following unwanted or unexpected effects: angioedema, peripheral motor neuropathy.

6096529-3 | Systemic Lupus Erythematosus
on Feb 25, 2009 Male patient from UNITED STATES , weighting 194.0 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Lialda (View Usage). Patient had the following side effects: systemic lupus erythematosus. Lialda dosage: 1.2 Gm 1 Time A Day.

6092138-0 | Multiple Sclerosis
on Feb 09, 2009 Female patient from UNITED STATES , 40 years of age, was diagnosed with inflammatory bowel disease and was treated with Lialda (View Usage). After Lialda was administered, patient had the following side effects: multiple sclerosis (What is multiple sclerosis?). Lialda dosage: 1.2 G, Oral. During the same period patient was treated with MERCAPTOPURINE (View Mercaptopurine Review and Mercaptopurine Label ), ATIVAN (View Ativan Review and Ativan Label ), KLOR CON (View Klor-con Review and Klor-con Label ).

6074871-X | Back Pain, Dyspnoea, Tremor
Patient was taking Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: back pain (What is back pain?), dyspnoea, tremor on Jan 29, 2009 from UNITED STATES Additional patient health information: Female patient , 49 years of age, weighting 220.0 lb, was diagnosed with colitis ulcerative and. Lialda dosage: Df, 2x/day, Bid; Oral. During the same period patient was treated with LYRICA (View Lyrica Review and Lyrica Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), BACLOFEN (View Baclofen Review and Baclofen Label ), PEROCET (OXYCODONE HYDROCHLORIDE, OXYCODONE TEREPHTHALATE, PARACETAMOL (View Perocet (oxycodone Hydrochloride, Oxycodone Terephthalate, Paracetamol Review and Perocet (oxycodone Hydrochloride, Oxycodone Terephthalate, Paracetamol Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), LUNESTA (View Lunesta Review and Lunesta Label ), NASACORT (View Nasacort Review and Nasacort Label ).

6067139-9 | Duodenal Ulcer Haemorrhage, Haematemesis
Adverse event was reported on Jan 19, 2009 by a Male patient taking Lialda (View Usage) (Dosage: 2.4 G Daily, Oral; 2.4 G Daily, Oral) was diagnosed with colitis ulcerative and. Location: UNITED STATES , 18 years of age, weighting 149.9 lb, Patient had the following side effects: duodenal ulcer haemorrhage, haematemesis. Patient was hospitalized.

6067136-3 | Atrial Fibrillation, Constipation, Faeces Hard, Fall
on Jan 20, 2009 Male patient from UNITED STATES , 86 years of age, weighting 173.9 lb, was diagnosed with colitis and was treated with Lialda (View Usage). After Lialda was administered, patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), constipation (What is constipation?), faeces hard, fall (What is fall?). Lialda dosage: See Image. During the same period patient was treated with IMODIUM /00384302/ (LOPERAMIDE HYDROCHLORIDE) (View Imodium /00384302/ (loperamide Hydrochloride) Review and Imodium /00384302/ (loperamide Hydrochloride) Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), POTASSIUM (POTASSIUM) (View Potassium (potassium) Review and Potassium (potassium) Label ), TENORMIN (View Tenormin Review and Tenormin Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

6052408-9 | Arrhythmia, Constipation, Faeces Hard, Fall
on Jan 09, 2009 Male patient from UNITED STATES , 86 years of age, weighting 173.9 lb, was diagnosed with colitis and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: arrhythmia (What is arrhythmia?), constipation (What is constipation?), faeces hard, fall (What is fall?). Lialda dosage: 1.2 G, 1x/day:qd, Oral; 2.4 G, 1x/day:qd, Oral. During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6026623-4 | Antinuclear Antibody Positive, Headache, Pyrexia
Patient was taking Lialda (View Usage). Patient had the following side effects: antinuclear antibody positive, headache (What is headache?), pyrexia on Dec 22, 2008 from UNITED STATES Additional patient health information: Female patient , 60 years of age, weighting 183.9 lb, was diagnosed with colitis and. Lialda dosage: 4.8 G, 1x/day:qd, Oral. Patient was hospitalized.

5960980-X | Gastroenteritis Viral, Myocarditis, Off Label Use
Adverse event was reported on Nov 04, 2008 by a Male patient taking Lialda (View Usage) (Dosage: 1x/day:qd, Oral) was diagnosed with crohn's disease (What is crohn's disease?) and. Location: UNITED STATES , 59 years of age, weighting 170.0 lb, After Lialda was administered, patient had the following side effects: gastroenteritis viral, myocarditis, off label use. During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), ACIPHEX (View Aciphex Review and Aciphex Label ), PREDNISONE (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

5960952-5 | Gallbladder Disorder, Hepatitis Acute, Off Label Use, Urinary Tract Infection
on Nov 11, 2008 Female patient from UNITED STATES , 41 years of age, was diagnosed with proctitis ulcerative and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: gallbladder disorder, hepatitis acute, off label use, urinary tract infection (What is urinary tract infection?). Lialda dosage: 2.4 G, 1x/day, Qd, Oral. Patient was hospitalized.

5955990-2 | Chest Pain, Stress
on Oct 30, 2008 Female patient from UNITED STATES , 42 years of age, weighting 181.9 lb, was diagnosed with proctitis ulcerative and was treated with Lialda (View Usage). Patient had the following side effects: chest pain (What is chest pain?), stress (What is stress?). Lialda dosage: 2.4 G, 2xday:bid, Oral. During the same period patient was treated with VICODIN (View Vicodin Review and Vicodin Label ), ELAVIL /00002202/ (AMITRIPTYLINE HYDROCHLORIDE) (View Elavil /00002202/ (amitriptyline Hydrochloride) Review and Elavil /00002202/ (amitriptyline Hydrochloride) Label ), ROWASA (View Rowasa Review and Rowasa Label ), TOPAMAX (View Topamax Review and Topamax Label ).

5939506-2 | Haematuria
Patient was taking Lialda (View Usage). After Lialda was administered, patient had the following side effects: haematuria on Oct 14, 2008 from UNITED STATES Additional patient health information: Male patient , 20 years of age, weighting 132.9 lb, was diagnosed with colitis ulcerative, crohn's disease (What is crohn's disease?) and. Lialda dosage: 4.8 G, 1x/day:qd,oral; 2.4 G, 1x/day:qd,oral;. During the same period patient was treated with PROTEIN SUPPLEMENTS (View Protein Supplements Review and Protein Supplements Label ).

5935193-8 | Influenza, Myocarditis
Adverse event was reported on Oct 16, 2008 by a Male patient taking Lialda (View Usage) (Dosage: 4.8 G, 1xday:qd, Oral) was diagnosed with colitis ulcerative and. Location: UNITED STATES , 43 years of age, weighting 265.0 lb, Patient experienced the following unwanted or unexpected effects: influenza, myocarditis. During the same period patient was treated with PROTONIX /01263201/ (PANTOPRAZOLE) (View Protonix /01263201/ (pantoprazole) Review and Protonix /01263201/ (pantoprazole) Label ). Patient was hospitalized.

5933494-0 | Blood Pressure Decreased, Heart Rate Decreased, Loss Of Consciousness
on Oct 10, 2008 Male patient from UNITED STATES , 84 years of age, weighting 181.9 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient had the following side effects: blood pressure decreased, heart rate decreased, loss of consciousness. Lialda dosage: 1.2 Df, 4x/day:qid, Oral. During the same period patient was treated with GLIPIZIDE (View Glipizide Review and Glipizide Label ). Patient was hospitalized.

5925246-2 | Chills, Hypotension, Nausea
on Oct 20, 2008 Male patient from UNITED STATES , 63 years of age, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). After Lialda was administered, patient had the following side effects: chills, hypotension, nausea (What is nausea?). Lialda dosage: . Patient was hospitalized.

5918341-5 | Caesarean Section, Colitis, Condition Aggravated, Gestational Diabetes, Pregnancy
Patient was taking Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: caesarean section, colitis, condition aggravated, gestational diabetes, pregnancy (What is pregnancy?) on Sep 30, 2008 from UNITED STATES Additional patient health information: Female patient , 20 years of age, weighting 104.9 lb, was diagnosed with colitis ulcerative and. Lialda dosage: 2.4g, 1x/day;qd;oral. During the same period patient was treated with PRENATAL VITAMINS(ASCORBIC ACID, BIOTIN, MINERALS NOS) (View Prenatal Vitamins(ascorbic Acid, Biotin, Minerals Nos) Review and Prenatal Vitamins(ascorbic Acid, Biotin, Minerals Nos) Label ), VITAMIN B12 (View Vitamin B12 Review and Vitamin B12 Label ).

5902641-9 | Abdominal Pain, Diarrhoea, Eating Disorder, Gait Disturbance, Haematochezia, Malaise, Off Label Use, Speech Disorder
Adverse event was reported on Sep 12, 2008 by a Female patient taking Lialda (View Usage) (Dosage: 3.6 G, 1x/day:qd, Oral) was diagnosed with crohn's disease (What is crohn's disease?) and. Location: UNITED STATES , 73 years of age, weighting 181.9 lb, Patient had the following side effects: abdominal pain (What is abdominal pain?), diarrhoea, eating disorder (What is eating disorder?), gait disturbance, haematochezia, malaise, off label use, speech disorder. During the same period patient was treated with HYZAAR (View Hyzaar Review and Hyzaar Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ).

5894486-3 | Anxiety, Bronchitis, Completed Suicide, Cough, Depression, Treatment Noncompliance
on Sep 08, 2008 Male patient from UNITED STATES , 54 years of age, weighting 259.9 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). After Lialda was administered, patient had the following side effects: anxiety (What is anxiety?), bronchitis (What is bronchitis?), completed suicide, cough, depression (What is depression?), treatment noncompliance. Lialda dosage: 4.8 G, 1x/day:gd, Oral. During the same period patient was treated with MULTIVITAMIN /00097801/ (ASCORBIC ACID, CALCIUM PANTOTHENATE, ERGOCALC (View Multivitamin /00097801/ (ascorbic Acid, Calcium Pantothenate, Ergocalc Review and Multivitamin /00097801/ (ascorbic Acid, Calcium Pantothenate, Ergocalc Label ), FISH OIL (FISH OIL) (View Fish Oil (fish Oil) Review and Fish Oil (fish Oil) Label ), ROZEREM (View Rozerem Review and Rozerem Label ), AVAPRO (View Avapro Review and Avapro Label ), CUTIVATE (FLUTICASONE PROPIONATE) (View Cutivate (fluticasone Propionate) Review and Cutivate (fluticasone Propionate) Label ).

5894414-0 | Aplastic Anaemia, Eating Disorder, Hypophagia, Stomatitis
on Sep 09, 2008 Female patient from UNITED STATES , 80 years of age, weighting 100.1 lb, was diagnosed with colitis and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: aplastic anaemia, eating disorder (What is eating disorder?), hypophagia, stomatitis. Lialda dosage: 1.2g, 1x/day:qd. Patient was hospitalized.

5877476-6 | Abasia, Anorexia, Aphasia, Asthenia, Fatigue, Feeling Abnormal, Frequent Bowel Movements, Off Label Use
Patient was taking Lialda (View Usage). Patient had the following side effects: abasia, anorexia, aphasia (What is aphasia?), asthenia, fatigue, feeling abnormal, frequent bowel movements, off label use on Aug 26, 2008 from UNITED STATES Additional patient health information: Female patient , 73 years of age, weighting 181.9 lb, was diagnosed with crohn's disease (What is crohn's disease?) and. Lialda dosage: 3.6 G, 1x/day:qd, Oral. During the same period patient was treated with HYZAAR /01284801/ (HYDROCHLOROTHIAZIDE,LOSARTAN POTASSIUM) (View Hyzaar /01284801/ (hydrochlorothiazide,losartan Potassium) Review and Hyzaar /01284801/ (hydrochlorothiazide,losartan Potassium) Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ).

5875730-5 | Condition Aggravated, Crohn's Disease, Gastritis, Lactose Intolerance, Off Label Use
Adverse event was reported on Aug 25, 2008 by a Female patient taking Lialda (View Usage) (Dosage: 3.6 G, 1x/day:qd, Oral) was diagnosed with crohn's disease (What is crohn's disease?) and. Location: UNITED STATES , 14 years of age, weighting 76.06 lb, After Lialda was administered, patient had the following side effects: condition aggravated, crohn's disease (What is crohn's disease?), gastritis, lactose intolerance (What is lactose intolerance?), off label use. During the same period patient was treated with REMICADE (View Remicade Review and Remicade Label ), IMURAN (View Imuran Review and Imuran Label ). Patient was hospitalized.

5875727-5 | Constipation, Dysgeusia, Hepatic Cyst, Hepatitis Acute, Pyrexia, Rash
on Aug 26, 2008 Female patient from UNITED STATES , 60 years of age, weighting 130.1 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: constipation (What is constipation?), dysgeusia, hepatic cyst, hepatitis acute, pyrexia, rash (What is rash?). Lialda dosage: 2.4 G, 2x/day:bid, Oral. During the same period patient was treated with EVISTA (View Evista Review and Evista Label ), LIPITOR (View Lipitor Review and Lipitor Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), GLUCOSAMINE (GLUCOSAMINE) (View Glucosamine (glucosamine) Review and Glucosamine (glucosamine) Label ), LEVBID (HYOSCYAMINE SULFATE) (View Levbid (hyoscyamine Sulfate) Review and Levbid (hyoscyamine Sulfate) Label ).

5853260-4 | Alopecia, Hypotension, Loss Of Consciousness, Off Label Use, Vomiting
on Aug 06, 2008 Female patient from UNITED STATES , 38 years of age, weighting 149.9 lb, was diagnosed with colitis, crohn's disease (What is crohn's disease?) and was treated with Lialda (View Usage). Patient had the following side effects: alopecia, hypotension, loss of consciousness, off label use, vomiting. Lialda dosage: 1.2 G, 2x/day: Bid, Oral. During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

5803959-0 | Pericarditis, Troponin Increased
Patient was taking Lialda (View Usage). After Lialda was administered, patient had the following side effects: pericarditis, troponin increased on Jun 20, 2008 from UNITED STATES Additional patient health information: Male patient , 22 years of age, was diagnosed with colitis ulcerative and. Lialda dosage: 4.8 G Daily, Oral. Patient was hospitalized.

5797460-0 | Dyspnoea, Pyrexia
Adverse event was reported on Jun 20, 2008 by a Male patient taking Lialda (View Usage) (Dosage: 2.4 G, Oral; 3.6 G Daily, Oral) was diagnosed with colitis ulcerative and. Location: UNITED STATES , 63 years of age, Patient experienced the following unwanted or unexpected effects: dyspnoea, pyrexia. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

5793274-6 | Pancreatitis Acute
on Jun 26, 2008 Female patient from UNITED STATES , weighting 146.0 lb, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient had the following side effects: pancreatitis acute. Lialda dosage: 4.8 Grams Daily Po. Patient was hospitalized.

5792731-6 | Colitis Collagenous, Condition Aggravated
on Jun 06, 2008 Male patient from UNITED STATES , 61 years of age, weighting 190.0 lb, was diagnosed with colitis collagenous and was treated with Lialda (View Usage). After Lialda was administered, patient had the following side effects: colitis collagenous, condition aggravated. Lialda dosage: 1.2 G, 2x/day: Bid, Oral. During the same period patient was treated with CLARITIN (View Claritin Review and Claritin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), TRIAMTERENE (TRIAMTERNE) (View Triamterene (triamterne) Review and Triamterene (triamterne) Label ), FLOMAX (View Flomax Review and Flomax Label ), VICODIN (View Vicodin Review and Vicodin Label ). Patient was hospitalized and became disabled.

5792678-5 | Hepatitis Acute
Patient was taking Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: hepatitis acute on Jun 13, 2008 from UNITED STATES Additional patient health information: Female patient , 60 years of age, weighting 130.1 lb, was diagnosed with colitis ulcerative and. Lialda dosage: 2.4 G, 2x/day:bid, Oral. During the same period patient was treated with EVISTA (View Evista Review and Evista Label ), LIPITOR (View Lipitor Review and Lipitor Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), GLUCOSAMINE (GLUCOSAMINE) (View Glucosamine (glucosamine) Review and Glucosamine (glucosamine) Label ), LEVBID (HYOSCYAMINE SULFATE) (View Levbid (hyoscyamine Sulfate) Review and Levbid (hyoscyamine Sulfate) Label ).

5788441-1 | Acute Febrile Neutrophilic Dermatosis
Adverse event was reported on Jun 06, 2008 by a Female patient taking Lialda (View Usage) (Dosage: 2.4 G, 1x/day;qd, Oral) was diagnosed with crohn's disease (What is crohn's disease?) and. Location: UNITED STATES , 44 years of age, weighting 136.0 lb, Patient had the following side effects: acute febrile neutrophilic dermatosis.

5773080-9 | Dyspnoea, Nonspecific Reaction, Pyrexia
on Jun 03, 2008 Male patient from UNITED STATES , 63 years of age, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). After Lialda was administered, patient had the following side effects: dyspnoea, nonspecific reaction, pyrexia. Lialda dosage: 2.4 G, 1x/day:qd,oral. During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

5773079-2 | Pericarditis
on Jun 03, 2008 Male patient from UNITED STATES , 22 years of age, was diagnosed with colitis ulcerative and was treated with Lialda (View Usage). Patient experienced the following unwanted or unexpected effects: pericarditis. Lialda dosage: 4.8 G, 1x/day:qd,oral. Patient was hospitalized.

5763799-8 | Chest Discomfort, Chest Pain
Patient was taking Lialda (View Usage). Patient had the following side effects: chest discomfort, chest pain (What is chest pain?) on May 23, 2008 from UNITED STATES Additional patient health information: Male patient , 68 years of age, weighting 179.9 lb, was diagnosed with colitis ulcerative and. Lialda dosage: 1.2 G, 1x/day:qd, Oral. Patient was hospitalized.

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Lialda Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

brenda   Location unknown

6:45pm on Thursday, April 2nd, 2009

are any of you women having any terrible rashes being exposed from your husband taking lialda?

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 Lialda 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 Lialda quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lialda 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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Lialda Reactions
Abdominal PainWhat is Abdominal pain?
Abdominal Pain Upper
Alanine Aminotransferase Increased
Alopecia
AnxietyWhat is Anxiety?
Arthralgia
Aspartate Aminotransferase Increased
Back PainWhat is Back pain?
Chest PainWhat is Chest pain?
Colitis Ulcerative
Condition Aggravated
ConstipationWhat is Constipation?
Crohn's DiseaseWhat is Crohn's disease?
Diarrhoea
Dyspepsia
Dyspnoea
FallWhat is Fall?
Fatigue
Feeling Abnormal
Haematochezia
Haematuria
Hepatitis Acute
Myalgia
Myocarditis
Off Label Use
Pancreatitis
Pancreatitis Acute
Pericarditis
Pyrexia
Vomiting
Lialda 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 Lialda 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!