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Lomotil adverse events reported to FDA.

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Summary

FDA Adverse Reports: 19. View All

Lomotil FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 5

Lomotil Dosage, Warnings, Usage.

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

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6974605-8 | Angioedema, Dyspnoea
on Sep 09, 2010 Female patient from UNITED STATES , 65 years of age, weighting 180.0 lb, was diagnosed with diarrhoea and was treated with Lomotil (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema, dyspnoea. Lomotil dosage: 2 Tabs Prn Po.

6890551-2 | Blood Pressure Decreased, Diarrhoea
Patient was taking Lomotil (View Usage). Patient had the following side effects: blood pressure decreased, diarrhoea on Nov 26, 2008 from UNITED STATES Additional patient health information: Male patient , 59 years of age, weighting 364.9 lb, was diagnosed with diarrhoea and. Lomotil dosage: Unk. During the same period patient was treated with LISINOPRIL (Unk) (View Lisinopril Review and Lisinopril Label ), IMODIUM (Unk) (View Imodium Review and Imodium Label ), METFORMIN HYDROCHLORIDE (500 Mg, 1x/day) (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ).

6890358-6 | Abdominal Pain
Adverse event was reported on Oct 06, 2008 by a Female patient taking Lomotil (View Usage) (Dosage: ) . Location: UNITED STATES , 76 years of age, weighting 165.0 lb, After Lomotil was administered, patient had the following side effects: abdominal pain (What is abdominal pain?). During the same period patient was treated with DIPHENOXYLATE HYDROCHLORIDE (View Diphenoxylate Hydrochloride Review and Diphenoxylate Hydrochloride Label ), ALDARA (View Aldara Review and Aldara Label ).

6889196-X | Erythema
on Jan 10, 2008 Female patient from UNITED STATES , weighting 176.0 lb, was diagnosed with diarrhoea, irritable bowel syndrome (What is irritable bowel syndrome?) and was treated with Lomotil (View Usage). Patient experienced the following unwanted or unexpected effects: erythema. Lomotil dosage: . During the same period patient was treated with DIAZIDE (View Diazide Review and Diazide Label ), ANTIBIOTICS (View Antibiotics Review and Antibiotics Label ).


6100388-X | Disability
on Feb 19, 2009 Male patient from UNITED STATES , 80 years of age, weighting 177.0 lb, was diagnosed with urinary tract disorder, cerebrovascular accident prophylaxis, nephrolithiasis, arrhythmia (What is arrhythmia?), hypertension and was treated with Lomotil (View Usage). Patient had the following side effects: disability. Lomotil dosage: . During the same period patient was treated with TAMSULOSIN (0.4 Mg, 1x/day) (View Tamsulosin Review and Tamsulosin Label ), DETROL LA (4 Mg, 1x/day) (View Detrol La Review and Detrol La Label ), ASPIRIN (81 Mg, 1x/day) (View Aspirin Review and Aspirin Label ), MULTI VITAMINS (Unk) (View Multi-vitamins Review and Multi-vitamins Label ), OSCAL (500 Mg, 2x/day) (View Oscal Review and Oscal Label ), PACERONE (400 Mg, 2x/day) (View Pacerone Review and Pacerone Label ), NORVASC (10 Mg, 1x/day) (View Norvasc Review and Norvasc Label ), METOPROLOL (50 Mg, 2x/day) (View Metoprolol Review and Metoprolol Label ).

6084318-5 | Dehydration
Patient was taking Lomotil (View Usage). After Lomotil was administered, patient had the following side effects: dehydration on Jan 28, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 231.5 lb, was diagnosed with crohn's disease (What is crohn's disease?) and. Lomotil dosage: Unk Mg/kg, Unk. During the same period patient was treated with REMICADE (5 Mg/kg, Unk) (View Remicade Review and Remicade Label ), LOPERAMIDE HYDROCHLORIDE (View Loperamide Hydrochloride Review and Loperamide Hydrochloride Label ), HUMIRA (View Humira Review and Humira Label ). Patient was hospitalized.

5918093-9 | Eating Disorder, Weight Decreased
Adverse event was reported on Oct 03, 2008 by a Male patient taking Lomotil (View Usage) (Dosage: ) was diagnosed with gastrointestinal disorder and. Location: BRAZIL , 43 years of age, Patient experienced the following unwanted or unexpected effects: eating disorder (What is eating disorder?), weight decreased.

5585231-X | Cholestasis, Hepatic Failure, Hepatic Fibrosis, Hypersexuality, Liver Injury
on Jan 08, 2008 Male patient from UNITED STATES , 28 years of age, was treated with Lomotil (View Usage). Patient had the following side effects: cholestasis, hepatic failure, hepatic fibrosis, hypersexuality, liver injury. Lomotil dosage: .

5545255-5 | Abdominal Pain, Nausea
on May 18, 2007 Female patient from UNITED STATES , 48 years of age, was diagnosed with breast cancer metastatic and was treated with Lomotil (View Usage). After Lomotil was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), nausea (What is nausea?). Lomotil dosage: . During the same period patient was treated with BELLADONNA EXTRACT (BELLADONNA EXTRACT) (View Belladonna Extract (belladonna Extract) Review and Belladonna Extract (belladonna Extract) Label ), LAPATINIB (LAPATINIB) (2500 Mg (1250 Mg, 2 In 1 D), Oral) (View Lapatinib (lapatinib) Review and Lapatinib (lapatinib) Label ), CAPECITABINE (CAPECITABINE) (3600 Mg (1800 Mg, 2 In 1 D), Oral) (View Capecitabine (capecitabine) Review and Capecitabine (capecitabine) Label ). Patient was hospitalized.

5163910-6 | Completed Suicide
Patient was taking Lomotil (View Usage). Patient experienced the following unwanted or unexpected effects: completed suicide on Nov 09, 2006 from UNITED STATES Additional patient health information: Female patient , 58 years of age, . Lomotil dosage: Oral. During the same period patient was treated with ACETAMINOPHEN AND HYDROCODONE BITARTRATE (Oral) (View Acetaminophen And Hydrocodone Bitartrate Review and Acetaminophen And Hydrocodone Bitartrate Label ), CLOPIDOGREL (Oral) (View Clopidogrel Review and Clopidogrel Label ).

5147010-7 | Blood Creatinine Increased, Dehydration, Gastroenteritis, Ileus, Mucosal Dryness, Mydriasis, Pharyngolaryngeal Pain, Rhinorrhoea, Somnolence
Adverse event was reported on Oct 13, 2006 by a Female patient taking Lomotil (View Usage) (Dosage: 2.5 Mg) was diagnosed with abdominal pain (What is abdominal pain?), vomiting and. Location: HONG KONG , child 7 years of age, Patient had the following side effects: blood creatinine increased, dehydration, gastroenteritis (What is gastroenteritis?), ileus, mucosal dryness, mydriasis, pharyngolaryngeal pain, rhinorrhoea, somnolence. During the same period patient was treated with LOPERAMIDE HCL (2 Mg (4 In 1 D)) (View Loperamide Hcl Review and Loperamide Hcl Label ), HYOSCINE HBR HYT (0.5 Mg (4 In 1 D)) (View Hyoscine Hbr Hyt Review and Hyoscine Hbr Hyt Label ), CHLORPHENIRAMINE (CHLORPHENIRAMINE) (4 Mg (4 In 1 D)) (View Chlorpheniramine (chlorpheniramine) Review and Chlorpheniramine (chlorpheniramine) Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

5053200-4 | Laboratory Test Abnormal
on Jun 29, 2006 Female patient from UNITED STATES , 26 years of age, weighting 250.0 lb, was diagnosed with diarrhoea and was treated with Lomotil (View Usage). After Lomotil was administered, patient had the following side effects: laboratory test abnormal. Lomotil dosage: 1 Capsule (4 In 1 D). During the same period patient was treated with PENICILLIN NOS (PENICILIN NOS) (View Penicillin Nos (penicilin Nos) Review and Penicillin Nos (penicilin Nos) Label ), MECLIZINE (View Meclizine Review and Meclizine Label ).

4942870-4 | Abnormal Behaviour, Agitation, Apathy, Constipation, Decreased Appetite, Delusion Of Reference, Euphoric Mood
on Feb 24, 2006 Male patient from INDIA , 40 years of age, was treated with Lomotil (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, agitation, apathy, constipation (What is constipation?), decreased appetite, delusion of reference, euphoric mood. Lomotil dosage: 25 To 30 Tablets 1 D.

4828374-8 | Abdominal Pain, Acute Sinusitis, Angina Pectoris, Arthralgia, Arthritis, Asthenia, Breast Mass, Bursitis, Carotid Artery Disease
Patient was taking Lomotil (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), acute sinusitis, angina pectoris, arthralgia, arthritis (What is arthritis?), asthenia, breast mass, bursitis (What is bursitis?), carotid artery disease (What is carotid artery disease?) on Jan 30, 2003 from UNITED STATES Additional patient health information: Female patient , 66 years of age, weighting 149.9 lb, was diagnosed with diarrhoea, sleep disorder (What is sleep disorder?), rheumatoid arthritis (What is rheumatoid arthritis?), diabetes mellitus, thyroid disorder and. Lomotil dosage: . During the same period patient was treated with PAMELOR (View Pamelor Review and Pamelor Label ), MELATONIN (View Melatonin Review and Melatonin Label ), AVANDIA (View Avandia Review and Avandia Label ), VIOXX (View Vioxx Review and Vioxx Label ), INSULIN (View Insulin Review and Insulin Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

4801891-2 | Diarrhoea, Gastrointestinal Motility Disorder
Adverse event was reported on Sep 28, 2005 by a Male patient taking Lomotil (View Usage) (Dosage: 2.5 Mg (2.5 Mg, 1 In 1 As Necessary), Oral) was diagnosed with frequent bowel movements and. Location: UNITED STATES , 80 years of age, weighting 162.0 lb, After Lomotil was administered, patient had the following side effects: diarrhoea, gastrointestinal motility disorder. During the same period patient was treated with MULTIVITAMIN (View Multivitamin Review and Multivitamin Label ), RETINOL (RETINOL) (View Retinol (retinol) Review and Retinol (retinol) Label ), VITAMIN C (VITAMIN C) (View Vitamin C (vitamin C) Review and Vitamin C (vitamin C) Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), COMPAZINE (View Compazine Review and Compazine Label ).

4778828-8 | Condition Aggravated, Multiple Sclerosis
on Sep 15, 2005 Male patient from CANADA , 29 years of age, was diagnosed with diarrhoea and was treated with Lomotil (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, multiple sclerosis (What is multiple sclerosis?). Lomotil dosage: Unk (qid Interval: Prn), Oral. During the same period patient was treated with TOPAMAX (View Topamax Review and Topamax Label ), COPAXONE (View Copaxone Review and Copaxone Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ), METAMUCIL 2 (View Metamucil-2 Review and Metamucil-2 Label ).

4765585-4 | Condition Aggravated, Multiple Sclerosis
on Aug 24, 2005 Male patient from CANADA , 29 years of age, was diagnosed with ill-defined disorder and was treated with Lomotil (View Usage). Patient had the following side effects: condition aggravated, multiple sclerosis (What is multiple sclerosis?). Lomotil dosage: Oral. During the same period patient was treated with TOPAMAX (View Topamax Review and Topamax Label ), COPAXONE (View Copaxone Review and Copaxone Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ), METAMUCIL ^SEARLE^ (PSYLLIUM HYDROPHILIC MUCILLOID) (View Metamucil ^searle^ (psyllium Hydrophilic Mucilloid) Review and Metamucil ^searle^ (psyllium Hydrophilic Mucilloid) Label ).

4733373-0 | Ileus Paralytic
Patient was taking Lomotil (View Usage). After Lomotil was administered, patient had the following side effects: ileus paralytic on Aug 01, 2005 from UNITED STATES Additional patient health information: Male patient , 76 years of age, was diagnosed with diarrhoea and. Lomotil dosage: 2 Q 6 H Prn. During the same period patient was treated with METRONIDAZOLE (View Metronidazole Review and Metronidazole Label ), PROMETHAZINE (View Promethazine Review and Promethazine Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), CALCIUM ACETATE (View Calcium Acetate Review and Calcium Acetate Label ), FINASTERIDE (View Finasteride Review and Finasteride Label ), HYDRALAZINE (View Hydralazine Review and Hydralazine Label ), BUPROPION (View Bupropion Review and Bupropion Label ). Patient was hospitalized.

4622814-5 | Abdominal Pain, Diarrhoea
Adverse event was reported on Mar 29, 2005 by a Female patient taking Lomotil (View Usage) (Dosage: One Po Qid Prn) was diagnosed with irritable bowel syndrome (What is irritable bowel syndrome?) and. Location: , 53 years of age, weighting 282.0 lb, Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), diarrhoea.


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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 Lomotil 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 Lomotil quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lomotil 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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Lomotil Reactions
Abdominal PainWhat is Abdominal pain?
Abnormal Behaviour
Acute Sinusitis
Agitation
Angina Pectoris
Angioedema
Apathy
Arthralgia
ArthritisWhat is Arthritis?
Asthenia
Blood Creatinine Increased
Blood Pressure Decreased
Breast Mass
BursitisWhat is Bursitis?
Carotid Artery DiseaseWhat is Carotid artery disease?
Cholestasis
Completed Suicide
Condition Aggravated
ConstipationWhat is Constipation?
Decreased Appetite
Dehydration
Delusion Of Reference
Diarrhoea
Disability
Dyspnoea
Eating DisorderWhat is Eating disorder?
Erythema
Euphoric Mood
GastroenteritisWhat is Gastroenteritis?
Multiple SclerosisWhat is Multiple sclerosis?
Lomotil 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 Lomotil 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!