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I was given 3 vials of Remicade last February 18, 2010 as treatment ...Keep Reading

I also recieved Remicade for my Ulcerative Colitis and after that I developed Alopecia ...Keep Reading

I have been on Remicade since last December 2009 ... it ...Keep Reading

Have been on Orencia several mo,s and developed lower leg edema 3+ and ...Keep Reading

Treated with Remicade for Ulcerative Colitis. Almost immediately developed Narcolepsy. Treatment discontinued,...Keep Reading

Wondering if there is an possibility that the 2 tooth abcesses I've had in ...Keep Reading

I am experiencing hair loss. I have had 4 remicade infusions ...Keep Reading

i have been diagnosed with crohn's disease since 1990. i have used many ...Keep Reading

I noticed that after my third Remicade treatment that my mood changed. I ...Keep Reading

I took remicade for five months for my RA and started with a very ...Keep Reading

I have been having kidney trouble, glomerulonephritis to be specific, it was ...Keep Reading

Same here, did your hair come back after stopping Remicade? andrealightfoot@msn.com...Keep Reading

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Indicate Your Remicade Side Effects
Depression (5)
Tooth Decay (4)
Mouth Sores (3)
Rash (3)
Cranial Nerve Palsy (2)
Hair Loss (2)
Nausea Amd Dizziness Flush Face (2)
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Common Remicade Side Effects

top 5 Remicade|Depression|Tooth deca|Mouth sore|Rash|Cranial ne|Hair loss|Nausea amd adverse effects>>See All Remicade Side Effects

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Remicade adverse events reported to FDA.

Have You Experienced unusual Remicade symptoms? PatientsVille.com collects and analyzes Remicade side effect and adverse reports submitted by Remicade users, such as Fatigue, diarrhea, nausea, joint pain, sore throat|eyeritis |atrial fibrillation |Invasive vaginal fungal infection, athletes foot, all|Flusing feeling in head, tightness in chest,|.

Summary

FDA Adverse Reports: 23439. View All

Remicade FDA safety alerts: 2001 2004 2008 2009

Reported deaths: 2435

Reported hospitalizations: 11005

More About Remicade

Post Your Unusual Symptoms:

Most Reported
1Depression
2Tooth Decay
3Chest Discomfort
4Rash
5Cranial Nerve Palsy
6Lung Infiltration
7Mouth Sores
8Tachycardia
9Tired
10Hair Loss
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Recent Drug Reports

Fatigue, diarrhea, nausea, joint pain, sore throat

eyeritis

atrial fibrillation

Invasive vaginal fungal infection, athletes foot, all

Flusing feeling in head, tightness in chest,

More Remicade Side Effect Reports

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

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7017735-7 | Abdominal Pain, Abscess, Back Pain, Condition Aggravated, Diarrhoea, Fatigue
on Sep 16, 2010 Male patient from CANADA , weighting 165.0 lb, was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), abscess (What is abscess?), back pain (What is back pain?), condition aggravated, diarrhoea, fatigue. Remicade dosage: . During the same period patient was treated with BENADRYL (View Benadryl Review and Benadryl Label ), TYLENOL (View Tylenol Review and Tylenol Label ), SOLU CORTEF (View Solu-cortef Review and Solu-cortef Label ).

7017723-0 | Anuria, Aspergillosis, Candida Sepsis, Cirrhosis Alcoholic, Device Related Infection, Hepatitis Alcoholic, Hepatitis B, Hypotension, Lactic Acidosis
Patient was taking Remicade (View Usage). Patient had the following side effects: anuria, aspergillosis, candida sepsis, cirrhosis alcoholic, device related infection, hepatitis alcoholic, hepatitis b (What is hepatitis b?), hypotension, lactic acidosis on Sep 16, 2010 from FRANCE Additional patient health information: Male patient , 58 years of age, was diagnosed with crohn's disease (What is crohn's disease?) and. Remicade dosage: . Patient was hospitalized.

7017722-9 | Excoriation, Fall, Pulse Absent, Red Blood Cell Count Decreased, White Blood Cell Count Decreased
Adverse event was reported on Sep 16, 2010 by a Male patient taking Remicade (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: CANADA , weighting 130.1 lb, After Remicade was administered, patient had the following side effects: excoriation, fall (What is fall?), pulse absent, red blood cell count decreased, white blood cell count decreased. During the same period patient was treated with METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), FERROUS SULFATE (View Ferrous Sulfate Review and Ferrous Sulfate Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), CALCIUM (View Calcium Review and Calcium Label ), ACTONEL (View Actonel Review and Actonel Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ). Patient was hospitalized.

7017717-5 | Antinuclear Antibody Positive, Asthenia, Hyperpyrexia, Infection, Myalgia, Nausea
on Sep 17, 2010 Female patient from FRANCE , 26 years of age, was diagnosed with hidradenitis (What is hidradenitis?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: antinuclear antibody positive, asthenia, hyperpyrexia, infection (What is infection?), myalgia, nausea (What is nausea?). Remicade dosage: 4 Doses.


7017716-3 | Hepatic Enzyme Increased, Muscular Weakness, Vision Blurred
on Sep 16, 2010 Female patient from UNITED STATES , weighting 200.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Remicade (View Usage). Patient had the following side effects: hepatic enzyme increased, muscular weakness, vision blurred. Remicade dosage: Every 4-6 Weeks. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ).

7017715-1 | Dementia Alzheimer's Type, Dyskinesia
Patient was taking Remicade (View Usage). After Remicade was administered, patient had the following side effects: dementia alzheimer's type, dyskinesia on Sep 16, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 223.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Remicade dosage: .

7017714-X | Thrombosis
Adverse event was reported on Sep 16, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with psoriasis and. Location: UNITED STATES , 50 years of age, Patient experienced the following unwanted or unexpected effects: thrombosis. During the same period patient was treated with STELARA (View Stelara Review and Stelara Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), SORIATANE (View Soriatane Review and Soriatane Label ), ENBREL (View Enbrel Review and Enbrel Label ), HUMIRA (View Humira Review and Humira Label ).

7017709-6 | Anal Fistula, Crohn's Disease
on Sep 16, 2010 Male patient from CANADA , weighting 125.2 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient had the following side effects: anal fistula, crohn's disease (What is crohn's disease?). Remicade dosage: .

7017708-4 | Dyspnoea, H1n1 Influenza
on Sep 16, 2010 Female patient from THAILAND , 71 years of age, weighting 132.3 lb, was diagnosed with psoriasis and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: dyspnoea, h1n1 influenza. Remicade dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ), NEOTIGASON (View Neotigason Review and Neotigason Label ). Patient was hospitalized.

7017707-2 | Arthritis Reactive, Intestinal Anastomosis, Pelvic Abscess, Resection Of Rectum, Surgery
Patient was taking Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: arthritis reactive, intestinal anastomosis, pelvic abscess, resection of rectum, surgery (What is surgery?) on Sep 15, 2010 from DENMARK Additional patient health information: Male patient , weighting 193.3 lb, was diagnosed with colitis ulcerative, abscess (What is abscess?), infection (What is infection?) and. Remicade dosage: . During the same period patient was treated with HUMIRA (View Humira Review and Humira Label ), CEFUROXIME (View Cefuroxime Review and Cefuroxime Label ), METRONIDAZOLE (View Metronidazole Review and Metronidazole Label ), CIPROXIN IV (View Ciproxin Iv Review and Ciproxin Iv Label ), CIPROXIN 500 (View Ciproxin 500 Review and Ciproxin 500 Label ), TAZOCIN (View Tazocin Review and Tazocin Label ), STEROIDS NOS (View Steroids Nos Review and Steroids Nos Label ). Patient was hospitalized.

7016154-7 | Ovarian Cancer
Adverse event was reported on Sep 16, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: JAPAN , weighting 158.7 lb, Patient had the following side effects: ovarian cancer. During the same period patient was treated with RHEUMATREX (View Rheumatrex Review and Rheumatrex Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ). Patient was hospitalized.

7016153-5 | Crohn's Disease
on Sep 15, 2010 Male patient from ITALY , weighting 105.2 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: crohn's disease (What is crohn's disease?). Remicade dosage: . During the same period patient was treated with 5 ASA (View 5-asa Review and 5-asa Label ). Patient was hospitalized.

7016132-8 | Enterococcal Infection, Multi-organ Failure, Renal Failure Acute, Respiratory Failure, Septic Shock
on Sep 16, 2010 Male patient from CANADA , 68 years of age, weighting 264.6 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), pain (What is pain?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: enterococcal infection, multi-organ failure, renal failure acute, respiratory failure, septic shock. Remicade dosage: . During the same period patient was treated with ARAVA (View Arava Review and Arava Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), CELEBREX (View Celebrex Review and Celebrex Label ), TYLENOL (View Tylenol Review and Tylenol Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), CRESTOR (View Crestor Review and Crestor Label ), NORVASC (View Norvasc Review and Norvasc Label ). Patient was hospitalized.

7016131-6 | Psoriatic Arthropathy
Patient was taking Remicade (View Usage). Patient had the following side effects: psoriatic arthropathy on Sep 16, 2010 from JAPAN Additional patient health information: Male patient , 52 years of age, . Remicade dosage: .

7016100-6 | Malignant Melanoma
Adverse event was reported on Sep 16, 2010 by a Female patient taking Remicade (View Usage) (Dosage: 3 Infusions (induction Phase)) was diagnosed with crohn's disease (What is crohn's disease?) and. Location: UNITED STATES , weighting 178.0 lb, After Remicade was administered, patient had the following side effects: malignant melanoma.

7016071-2 | Depression, Haematochezia, Salmonellosis
on Jun 03, 2010 Male patient from COLOMBIA , 46 years of age, was diagnosed with colitis ulcerative and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: depression (What is depression?), haematochezia, salmonellosis. Remicade dosage: . During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), MESALAZINE (View Mesalazine Review and Mesalazine Label ), AZATHIOPRINE (View Azathioprine Review and Azathioprine Label ), CALCITRIOL (View Calcitriol Review and Calcitriol Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ). Patient was hospitalized.

7016070-0 | Fall, Humerus Fracture
on Sep 16, 2010 Female patient from CANADA , weighting 132.7 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient had the following side effects: fall (What is fall?), humerus fracture. Remicade dosage: . Patient was hospitalized.

7016052-9 | Tuberculosis
Patient was taking Remicade (View Usage). After Remicade was administered, patient had the following side effects: tuberculosis (What is tuberculosis?) on Jun 03, 2010 from COLOMBIA Additional patient health information: Male patient , 40 years of age, was diagnosed with psoriasis and. Remicade dosage: . Patient was hospitalized.

7016043-8 | Lung Disorder
Adverse event was reported on Sep 16, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: SWEDEN , 73 years of age, Patient experienced the following unwanted or unexpected effects: lung disorder. Patient was hospitalized.

7016042-6 | Adverse Event, Arthralgia, Hyperhidrosis, Shoulder Operation, Stomatitis
on Sep 16, 2010 Female patient from UNITED STATES , weighting 168.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), hypertension, thyroid disorder and was treated with Remicade (View Usage). Patient had the following side effects: adverse event, arthralgia, hyperhidrosis, shoulder operation, stomatitis. Remicade dosage: . During the same period patient was treated with BENADRYL (View Benadryl Review and Benadryl Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), THYROID (View Thyroid Review and Thyroid Label ).

7016041-4 | Meningitis
on Sep 16, 2010 Female patient from ECUADOR , 51 years of age, was diagnosed with dermatomyositis and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: meningitis (What is meningitis?). Remicade dosage: . Patient was hospitalized.

7015575-6 | B-cell Lymphoma, Back Pain, Urticaria
Patient was taking Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: b-cell lymphoma, back pain (What is back pain?), urticaria on Sep 16, 2010 from JAPAN Additional patient health information: Male patient , weighting 138.9 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Remicade dosage: 23rd Dose. During the same period patient was treated with RHEUMATREX (View Rheumatrex Review and Rheumatrex Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), VOLTAREN (View Voltaren Review and Voltaren Label ), AZELASTINE HCL (View Azelastine Hcl Review and Azelastine Hcl Label ), TAKEPRON (View Takepron Review and Takepron Label ), BONALON (View Bonalon Review and Bonalon Label ). Patient was hospitalized.

7015537-9 | Headache
Adverse event was reported on Sep 16, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with inflammatory bowel disease and. Location: UNITED STATES , weighting 141.3 lb, Patient had the following side effects: headache (What is headache?). During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ), IRON (View Iron Review and Iron Label ), TOPAMAX (View Topamax Review and Topamax Label ), 5 ASA (View 5-asa Review and 5-asa Label ). Patient was hospitalized.

7015478-7 | Blood Urine Present, Cardiac Arrest, Cerebrovascular Accident, Convulsion, Fall, Haematochezia, International Normalised Ratio Increased
on Sep 16, 2010 Male patient from UNITED STATES , weighting 167.0 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: blood urine present, cardiac arrest (What is cardiac arrest?), cerebrovascular accident, convulsion, fall (What is fall?), haematochezia, international normalised ratio increased. Remicade dosage: 8 Infusions Prior To Baseline. During the same period patient was treated with ANTIDEPRESSANTS (View Antidepressants Review and Antidepressants Label ), BUDESONIDE (View Budesonide Review and Budesonide Label ), NARCOTIC ANALGESICS, NOS (View Narcotic Analgesics, Nos Review and Narcotic Analgesics, Nos Label ). Patient was hospitalized.

7015477-5 | Arthralgia, Stress
on Sep 16, 2010 Female patient from CANADA , weighting 255.7 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, stress (What is stress?). Remicade dosage: .

7015476-3 | Impaired Healing, Ovarian Cyst
Patient was taking Remicade (View Usage). Patient had the following side effects: impaired healing, ovarian cyst (What is ovarian cyst?) on Sep 16, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 135.0 lb, was diagnosed with crohn's disease (What is crohn's disease?) and. Remicade dosage: .

7015463-5 | Glomerulonephritis Rapidly Progressive, Renal Failure Chronic
Adverse event was reported on Sep 15, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: JAPAN , 35 years of age, After Remicade was administered, patient had the following side effects: glomerulonephritis rapidly progressive, renal failure chronic. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), ETANERCEPT (View Etanercept Review and Etanercept Label ), NSAID (View Nsaid Review and Nsaid Label ), SULFASALAZINE (View Sulfasalazine Review and Sulfasalazine Label ).

7015461-1 | Arthropathy, Candida Test Positive, Disseminated Intravascular Coagulation, Flavobacterium Test Positive, Hyperthermia Malignant, Interstitial Lung Disease, Respiratory Failure, Staphylococcal Infection
on Sep 15, 2010 Female patient from JAPAN , 63 years of age, weighting 114.6 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), gastritis, constipation (What is constipation?), tinea infection (What is tinea infection?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: arthropathy, candida test positive, disseminated intravascular coagulation, flavobacterium test positive, hyperthermia malignant, interstitial lung disease, respiratory failure, staphylococcal infection (What is staphylococcal infection?). Remicade dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), MAGLAX (View Maglax Review and Maglax Label ), ALOSENN (View Alosenn Review and Alosenn Label ), LAMISIL (View Lamisil Review and Lamisil Label ).

7015460-X | Decreased Appetite, Nausea, Umbilical Hernia, Weight Decreased
on Sep 16, 2010 Male patient from CANADA , weighting 224.9 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient had the following side effects: decreased appetite, nausea (What is nausea?), umbilical hernia, weight decreased. Remicade dosage: . Patient was hospitalized.

7015459-3 | Malaise, Pyrexia
Patient was taking Remicade (View Usage). After Remicade was administered, patient had the following side effects: malaise, pyrexia on Sep 16, 2010 from PERU Additional patient health information: Male patient , 47 years of age, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and. Remicade dosage: .

7015458-1 | Head Injury, Hypotension, Loss Of Consciousness
Adverse event was reported on Sep 16, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: UNITED STATES , weighting 160.0 lb, Patient experienced the following unwanted or unexpected effects: head injury, hypotension, loss of consciousness. Patient was hospitalized.

7015341-1 | Choroid Melanoma
on Sep 16, 2010 Male patient from BELGIUM , 64 years of age, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and was treated with Remicade (View Usage). Patient had the following side effects: choroid melanoma. Remicade dosage: . Patient was hospitalized.

7015340-X | Nervous System Disorder
on Sep 15, 2010 Female patient from UNITED KINGDOM , 32 years of age, was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: nervous system disorder. Remicade dosage: .

7015242-9 | Cardiac Failure, Congestive Cardiomyopathy, Renal Impairment, Supraventricular Tachycardia
Patient was taking Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac failure, congestive cardiomyopathy, renal impairment, supraventricular tachycardia on Sep 15, 2010 from JAPAN Additional patient health information: Male patient , weighting 136.7 lb, was diagnosed with crohn's disease (What is crohn's disease?) and. Remicade dosage: Total Of 2 Infusions. During the same period patient was treated with IMURAN (View Imuran Review and Imuran Label ), PENTASA (View Pentasa Review and Pentasa Label ), FLAGYL (View Flagyl Review and Flagyl Label ), TAKEPRON (View Takepron Review and Takepron Label ). Patient was hospitalized.

7014766-8 | Influenza Like Illness, Osteoarthritis
Adverse event was reported on Sep 15, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), cough and. Location: CANADA , weighting 154.3 lb, Patient had the following side effects: influenza like illness, osteoarthritis (What is osteoarthritis?). During the same period patient was treated with BIAXIN (View Biaxin Review and Biaxin Label ), UROZIDE (View Urozide Review and Urozide Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ), FOSAMAX (View Fosamax Review and Fosamax Label ).

7014670-5 | Epistaxis, Escherichia Infection, Feeling Abnormal, Therapeutic Response Decreased
on Sep 15, 2010 Female patient from UNITED STATES , weighting 220.0 lb, was diagnosed with psoriasis, pain (What is pain?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: epistaxis, escherichia infection, feeling abnormal, therapeutic response decreased. Remicade dosage: . During the same period patient was treated with ALEVE (CAPLET) (View Aleve (caplet) Review and Aleve (caplet) Label ), MOTRIN (View Motrin Review and Motrin Label ).

7014666-3 | Amnesia, Body Height Decreased, Bronchitis, Osteogenesis Imperfecta, Rash Macular, Spinal Operation
on Sep 15, 2010 Female patient from UNITED STATES , weighting 140.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), osteoarthritis (What is osteoarthritis?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: amnesia, body height decreased, bronchitis (What is bronchitis?), osteogenesis imperfecta (What is osteogenesis imperfecta?), rash macular, spinal operation. Remicade dosage: . During the same period patient was treated with RECLAST (View Reclast Review and Reclast Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ). Patient was hospitalized.

7014569-4 | Condition Aggravated, Crohn's Disease, Disease Complication, Dyspnoea, Headache, Infusion Related Reaction, Rash, Skin Reaction
Patient was taking Remicade (View Usage). Patient had the following side effects: condition aggravated, crohn's disease (What is crohn's disease?), disease complication, dyspnoea, headache (What is headache?), infusion related reaction, rash (What is rash?), skin reaction on Sep 24, 2010 from UNITED STATES Additional patient health information: Male patient , 24 years of age, was diagnosed with crohn's disease (What is crohn's disease?) and. Remicade dosage: 500 Mg Week 0, 2, And 6 Iv Drip. Patient was hospitalized.

7014444-5 | Dyspnoea, Infusion Related Reaction, Pyrexia, Sensation Of Pressure
Adverse event was reported on Sep 15, 2010 by a Male patient taking Remicade (View Usage) (Dosage: ) was diagnosed with crohn's disease (What is crohn's disease?) and. Location: JAPAN , weighting 134.5 lb, After Remicade was administered, patient had the following side effects: dyspnoea, infusion related reaction, pyrexia, sensation of pressure. During the same period patient was treated with CORTICOSTEROIDS NOS (View Corticosteroids Nos Review and Corticosteroids Nos Label ).

7014441-X | Haematochezia
on Sep 15, 2010 Female patient from CANADA , weighting 155.4 lb, was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: haematochezia. Remicade dosage: . During the same period patient was treated with IMURAN (View Imuran Review and Imuran Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), LOPERAMIDE (View Loperamide Review and Loperamide Label ), BACLOFEN (View Baclofen Review and Baclofen Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), PANTOLOC (View Pantoloc Review and Pantoloc Label ). Patient was hospitalized.

7014440-8 | Abdominal Pain Upper, Cellulitis, Dental Caries, Fungal Oesophagitis, Sjogren's Syndrome, Tooth Fracture
on Sep 15, 2010 Female patient from UNITED STATES , weighting 127.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), gastrooesophageal reflux disease, bone density abnormal, blood cholesterol, depression (What is depression?), migraine (What is migraine?), pain (What is pain?), muscle spasms and was treated with Remicade (View Usage). Patient had the following side effects: abdominal pain upper, cellulitis (What is cellulitis?), dental caries, fungal oesophagitis, sjogren's syndrome (What is sjogren's syndrome?), tooth fracture. Remicade dosage: . During the same period patient was treated with PREVACID (View Prevacid Review and Prevacid Label ), EVISTA (View Evista Review and Evista Label ), PRAVACHOL (View Pravachol Review and Pravachol Label ), LOPID (View Lopid Review and Lopid Label ), EFFEXOR (View Effexor Review and Effexor Label ), RELPAX (View Relpax Review and Relpax Label ), VICODIN (View Vicodin Review and Vicodin Label ), FLEXERIL (View Flexeril Review and Flexeril Label ).

7014439-1 | Fungal Infection, Lymphocyte Count, Neutrophilia
Patient was taking Remicade (View Usage). After Remicade was administered, patient had the following side effects: fungal infection (What is fungal infection?), lymphocyte count, neutrophilia on Sep 16, 2010 from FRANCE Additional patient health information: Male patient , 60 years of age, was diagnosed with erythrodermic psoriasis and. Remicade dosage: . Patient was hospitalized.

7014341-5 | Malaise, Oedema Peripheral, Pain In Extremity
Adverse event was reported on Sep 15, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with psoriasis, pain (What is pain?) and. Location: UNITED STATES , weighting 260.0 lb, Patient experienced the following unwanted or unexpected effects: malaise, oedema peripheral, pain in extremity. During the same period patient was treated with CELEBREX (View Celebrex Review and Celebrex Label ), PERCOCET (View Percocet Review and Percocet Label ). Patient was hospitalized.

7014340-3 | Fall, Upper Limb Fracture
on Sep 15, 2010 Female patient from CANADA , weighting 197.3 lb, was diagnosed with colitis ulcerative and was treated with Remicade (View Usage). Patient had the following side effects: fall (What is fall?), upper limb fracture. Remicade dosage: . During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

7014339-7 | Anxiety, Back Pain, Chest Pain, Colitis, Infusion Related Reaction
on Sep 15, 2010 Female patient from UNITED STATES , weighting 140.0 lb, was diagnosed with colitis ulcerative, pain (What is pain?), thyroid disorder and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: anxiety (What is anxiety?), back pain (What is back pain?), chest pain (What is chest pain?), colitis, infusion related reaction. Remicade dosage: . During the same period patient was treated with TYLENOL (View Tylenol Review and Tylenol Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), BENADRYL (View Benadryl Review and Benadryl Label ).

7014269-0 | Disseminated Tuberculosis, Sepsis
Patient was taking Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: disseminated tuberculosis, sepsis (What is sepsis?) on Sep 15, 2010 from CANADA Additional patient health information: Male patient , weighting 147.7 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Remicade dosage: . During the same period patient was treated with BENADRYL (View Benadryl Review and Benadryl Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), ARAVA (View Arava Review and Arava Label ). Patient was hospitalized.

7014267-7 | Blood Pressure Increased, Breast Pain, Infusion Related Reaction, Memory Impairment
Adverse event was reported on Sep 15, 2010 by a Male patient taking Remicade (View Usage) (Dosage: ) was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and. Location: BRAZIL , 21 years of age, Patient had the following side effects: blood pressure increased, breast pain, infusion related reaction, memory impairment.

7014266-5 | Ovarian Cyst, Vaginal Cyst
on Sep 15, 2010 Female patient from CANADA , 52 years of age, weighting 115.3 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: ovarian cyst (What is ovarian cyst?), vaginal cyst. Remicade dosage: . During the same period patient was treated with ACTONEL (View Actonel Review and Actonel Label ), PANTOLOC (View Pantoloc Review and Pantoloc Label ), VITAMIN B 12 (View Vitamin B-12 Review and Vitamin B-12 Label ).

7014264-1 | Cytomegalovirus Infection
on Sep 16, 2010 Male patient from UNITED STATES , child 10 years of age, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: cytomegalovirus infection (What is cytomegalovirus infection?). Remicade dosage: . During the same period patient was treated with AZATHIOPRINE (View Azathioprine Review and Azathioprine Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ).

7014263-X | Lymphadenopathy, Night Sweats, Pyrexia, Rash
Patient was taking Remicade (View Usage). Patient had the following side effects: lymphadenopathy, night sweats, pyrexia, rash (What is rash?) on Sep 15, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 120.0 lb, was diagnosed with crohn's disease (What is crohn's disease?) and. Remicade dosage: .

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Remicade Questions, Answers, Feedback and Comments

Comments to date: 5. Page 1 of 1.

Tamara   Mesa, Arizona

11:20pm on Saturday, April 23rd, 2011


I have ulcerative colitis, I have had 9 treatments of Remicade and have decided to stop. I have a... read more »

Lavonna   oakhurst 

12:38pm on Friday, December 3rd, 2010

Put on Remicade for non FDA approved disease called hidradenitis, mine is severe, but, i never got b... read more »

Nathalie   Metro Manila

6:04am on Sunday, February 28th, 2010

I recieved Remicade as treatment for my Ulcerative Colitis and after the treatment my diarrhea has w... read more »

Gail James   Location unknown

4:02am on Thursday, November 20th, 2008

I have been on Remicade since July 08. I have had many skin rash-like outbreaks, like psoriasis and ... read more »

Carol Beaulieu   Location unknown

3:32pm on Friday, September 5th, 2008

Remicade treatments in 2003 for Crohn's disease. During administration of my third dose, I immediat... 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 Remicade 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 Remicade quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Remicade 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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Remicade Reactions
Abdominal PainWhat is Abdominal pain?
Arthralgia
Asthenia
Back PainWhat is Back pain?
Breast CancerWhat is Breast cancer?
Chest Discomfort
Chest PainWhat is Chest pain?
Chills
Crohn's DiseaseWhat is Crohn's disease?
Death
Diarrhoea
Disseminated Tuberculosis
DizzinessWhat is Dizziness?
Dyspnoea
FallWhat is Fall?
Fatigue
Flushing
HeadacheWhat is Headache?
Infusion Related Reaction
Lupus-like Syndrome
Malaise
NauseaWhat is Nausea?
Pneumocystis Jiroveci Pneumonia
PneumoniaWhat is Pneumonia?
Pulmonary Tuberculosis
Pyrexia
RashWhat is Rash?
SepsisWhat is Sepsis?
TuberculosisWhat is Tuberculosis?
Vomiting
Remicade 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 Remicade 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!