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Imodium (Loperamide) - Reports of Side Effects & Adverse Reactions

 


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This is an index of adverse event reports related to Imodium (Loperamide). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the adverse reaction. Or scroll down to view a sample of recent reports further on this page.

Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.

All cases (39)
     Renal Failure Acute (4)Intentional Drug Misuse (3)Flushing (3)more >>

Cases resulting in a serious event (37)
     Renal Failure Acute (4)Intentional Drug Misuse (3)Flushing (3)more >>

Cases resulting in death (2)
     Skin Disorder (1)Diarrhoea (1)

Cases resulting in hospitalization (13)
     Renal Failure Acute (4)Rash Pustular (2)Pancytopenia (2)more >>

Cases resulting in disability (3)
     Flushing (3)

Cases resulting in other serious reactions (21)
     Urinary Retention (3)Abdominal Pain (2)Prostate Examination Abnormal (2)more >>

Below is a sample of adverse event reports reports related to Imodium (Loperamide). For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in 11 year old male receiving Imodium (Loperamide)

Reported by a consumer/non-health professional from United States on 2007-10-31

Patient: 11 year old male

Adverse reactions / side effects: Weight Decreased, Abdominal Pain, Productive Cough, Headache, Abdominal Tenderness, Gastritis, Malaise, Pharyngolaryngeal Pain, Dizziness, Blindness Transient, Viral Infection, Vomiting, Nausea, Rhinorrhoea, Diarrhoea, Anorexia, Sinus Headache, Gastroduodenitis

Suspect drug(s):
Listerine Agent Cool Blue Glacier Mint (NO Active Ingredient
    Dosage: oral
    Administration route: Oral
    Start date: 2007-02-06

Imodium
    Dosage: 1-2 oid prn (12.5 mg), ophthalmic
    Indication: Diarrhoea

Phenergan (Promethazine Hydrochloride)
    Dosage: 1 qid prn (2 mg, 1 in 1 d), oral
    Administration route: Oral
    Indication: Nausea



Adverse event in receiving Imodium (Loperamide)

Reported by a physician from United Kingdom on 2007-10-29

Patient:

Adverse reactions / side effects: Premature Baby, Drug Exposure During Pregnancy

Suspect drug(s):
Imodium (Loperamide)



Adverse event in female receiving Imodium (Loperamide)

Reported by a physician from United Kingdom on 2007-10-24

Patient: female

Adverse reactions / side effects: Drug Exposure During Pregnancy, Vaginal Discharge, Premature Labour

Suspect drug(s):
Imodium (Loperamide)



Adverse event in male receiving Imodium (Loperamide)

Reported by a consumer/non-health professional from United Kingdom on 2007-10-23

Patient: male

Adverse reactions / side effects: Death

Adverse event resulted in: death

Suspect drug(s):
Bevacizumab
    Dosage: 450 mg, q2w
    Indication: Gastric Cancer
    Start date: 2007-06-13

Erlotinib
    Dosage: 150 mg, qd
    Administration route: Oral
    Indication: Gastric Cancer
    Start date: 2007-06-13

Duragesic-100
    Dosage: 125 a?g, qd
    Indication: Pain
    Start date: 2007-08-01

Duragesic-100
    Dosage: 100 a?g, qd
    Start date: 2007-06-13
    End date: 2007-08-01

Duragesic-100
    Dosage: 75 a?g, qd
    Start date: 2007-06-07
    End date: 2007-06-13

Duragesic-100
    Dosage: 50 a?g, qd
    End date: 2007-06-07

Acetaminophen
    Dosage: 4000 mg, qd
    Indication: Pain
    Start date: 2007-08-08

Acetaminophen
    Dosage: 1000 mg, prn
    Administration route: Oral
    Start date: 2007-08-08
    End date: 2007-08-08

Morphine
    Dosage: 30 mg, prn
    Administration route: Oral
    Indication: Pain

Imodium
    Dosage: 1 mg, prn
    Administration route: Oral
    Indication: Diarrhoea
    Start date: 2007-06-27

Prednisolone
    Dosage: 25 mg, qd
    Administration route: Oral
    Indication: Nausea
    Start date: 2007-07-10

Supplement NOS
    Administration route: Oral
    Indication: Weight Decreased
    Start date: 2007-06-27

Gabapentin
    Dosage: 900 mg, qd
    Administration route: Oral
    Indication: Pain
    Start date: 2007-08-08
    End date: 2007-08-13

Gabapentin
    Dosage: 1800 mg, qd
    Administration route: Oral
    End date: 2007-08-08

Metadon
    Dosage: 90 mg, qd
    Administration route: Oral
    Indication: Pain



Adverse event in female receiving Imodium (Loperamide)

Reported by a physician from Germany on 2007-10-17

Patient: female

Adverse reactions / side effects: Fatigue, Intentional Drug Misuse, Aggression

Adverse event resulted in: hospitalization

Suspect drug(s):
Imodium
    Dosage: dose unknown
    Indication: Suicide Attempt

Fluanxol
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ibuprofen
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Infectocillin
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Kytta
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Novalgin
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Vivinox
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in 20 year old male receiving Imodium (Loperamide)

Reported by a physician from Germany on 2007-10-17

Patient: 20 year old male, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Intentional Overdose, Restlessness, Tachycardia, Disorientation

Suspect drug(s):
Imodium
    Administration route: Oral
    Indication: Suicide Attempt

Cotrim DS
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Emesan
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Mega Penicillin
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in male receiving Imodium (Loperamide)

Reported by a consumer/non-health professional from United Kingdom on 2007-10-02

Patient: male

Adverse reactions / side effects: Death, Diarrhoea, Skin Disorder

Adverse event resulted in: death

Suspect drug(s):
Bevacizumab
    Dosage: 450 mg, q2w
    Indication: Gastric Cancer
    Start date: 2007-06-13

Erlotinib
    Dosage: 150 mg, qd
    Administration route: Oral
    Indication: Gastric Cancer
    Start date: 2007-06-13

Duragesic-100
    Dosage: 125 a?g, qd
    Indication: Pain
    Start date: 2007-08-01

Duragesic-100
    Dosage: 100 a?g, qd
    Start date: 2007-06-13
    End date: 2007-08-01

Duragesic-100
    Dosage: 75 a?g, qd
    Start date: 2007-06-07
    End date: 2007-06-13

Duragesic-100
    Dosage: 50 a?g, qd
    End date: 2007-06-07

Acetaminophen
    Dosage: 4000 mg, qd
    Indication: Pain
    Start date: 2007-08-08

Acetaminophen
    Dosage: 1000 mg, prn
    Administration route: Oral
    Start date: 2007-08-08
    End date: 2007-08-08

Morphine
    Dosage: 30 mg, prn
    Administration route: Oral
    Indication: Pain

Imodium
    Dosage: 1 mg, prn
    Administration route: Oral
    Indication: Diarrhoea
    Start date: 2007-06-27

Prednisolone
    Dosage: 25 mg, qd
    Administration route: Oral
    Indication: Nausea
    Start date: 2007-07-10

Supplement NOS
    Administration route: Oral
    Indication: Weight Decreased
    Start date: 2007-06-27

Gabapentin
    Dosage: 900 mg, qd
    Administration route: Oral
    Indication: Pain
    Start date: 2007-08-08
    End date: 2007-08-13

Gabapentin
    Dosage: 1800 mg, qd
    Administration route: Oral
    End date: 2007-08-08

Metadon
    Dosage: 90 mg, qd
    Administration route: Oral
    Indication: Pain



Adverse event in male receiving Imodium (Loperamide)

Reported by a physician from United Kingdom on 2007-07-17

Patient: male

Adverse reactions / side effects: Anaemia Haemolytic Autoimmune

Suspect drug(s):
Imodium (Loperamide)



Adverse event in female receiving Imodium (Loperamide)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-17

Patient: female

Adverse reactions / side effects: Megacolon, Large Intestine Perforation, Amoebic Colitis, Lymphopenia, Hyponatraemia, Gastrointestinal Necrosis, Ileus Paralytic, Sepsis, Hypoalbuminaemia, Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Imodium (Loperamide)

Other drugs received by patient: Rifaximin; Levothyroxine Sodium



Adverse event in male receiving Imodium (Loperamide)

Reported by a physician from Italy on 2007-07-06

Patient: male

Adverse reactions / side effects: Abdominal Pain, Nausea, Headache, Staring, Tremor, Loss of Consciousness

Suspect drug(s):
Imodium (Loperamide)

Other drugs received by patient: Paracetamol



Adverse event in 28 year old female receiving Imodium (Loperamide)

Reported by a consumer/non-health professional from Germany on 2007-06-29

Patient: 28 year old female

Adverse reactions / side effects: Drug Abuser, Drug Interaction, Drug Withdrawal Syndrome

Suspect drug(s):
Imodium
    Administration route: Oral

Imodium
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient possibly interacting with the suspect drug:
Homeopathic Injection
    Indication: Detoxification



Adverse event in 92 year old female receiving Imodium (Loperamide)

Reported by a physician from France on 2007-06-28

Patient: 92 year old female

Adverse reactions / side effects: Intestinal Obstruction

Suspect drug(s):
Imodium
    Indication: Constipation

Imodium
    Indication: Diarrhoea



Adverse event in female receiving Imodium (Loperamide)

Reported by a physician from Germany on 2007-06-19

Patient: female, weighing 50.0 kg (110.0 pounds)

Adverse reactions / side effects: Suicide Attempt

Suspect drug(s):
Imodium
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Fenistil
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in male receiving Imodium (Loperamide)

Reported by a consumer/non-health professional from United Kingdom on 2007-06-15

Patient: male

Adverse reactions / side effects: Drug Ineffective, Arthritis Reactive, Expired Drug Administered

Suspect drug(s):
Imodium (Loperamide)



Adverse event in 68 year old female receiving Imodium (Loperamide)

Reported by a individual with unspecified qualification from United States on 2007-06-07

Patient: 68 year old female

Adverse reactions / side effects: Vomiting, Diarrhoea, Unevaluable Event

Adverse event resulted in: hospitalization

Suspect drug(s):
Imodium
    Dosage: oral
    Administration route: Oral
    Indication: Diarrhoea
    Start date: 2007-05-01
    End date: 2007-05-11

Acetaminophen
    Dosage: oral
    Administration route: Oral
    Start date: 2007-05-01
    End date: 2007-05-11

Loratadine
    Dosage: oral
    Administration route: Oral
    Indication: Cough
    Start date: 2007-05-01
    End date: 2007-05-11

Mucinex DM
    Indication: Cough



Adverse event in 3 year old female receiving Imodium (Loperamide)

Reported by a health professional (non-physician/pharmacist) from Belgium on 2007-05-21

Patient: 3 year old female, weighing 15.7 kg (34.5 pounds)

Adverse reactions / side effects: Confusional State, Vertigo, Somnolence

Adverse event resulted in: hospitalization

Suspect drug(s):
Imodium (Loperamide)



Adverse event in 57 year old female receiving Imodium (Loperamide)

Reported by a health professional (non-physician/pharmacist) from France on 2007-05-21

Patient: 57 year old female, weighing 87.0 kg (191.4 pounds)

Adverse reactions / side effects: Pancytopenia, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Imodium
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Glucophage
    Administration route: Oral
    Indication: Diabetes Mellitus non-Insulin-Dependent

Lytos
    Indication: Drug USE FOR Unknown Indication

Alimta

Alimta
    Indication: Drug USE FOR Unknown Indication

Tarceva
    Indication: Lung Adenocarcinoma

Micardis
    Indication: Hypertension

Other drugs received by patient: Folic Acid; Vitamin B-12; Aluminum Hydroxide and Magnesium Trisilicate



Adverse event in 57 year old female receiving Imodium (Loperamide)

Reported by a health professional (non-physician/pharmacist) from Germany on 2007-05-21

Patient: 57 year old female

Adverse reactions / side effects: Systemic Candida, Pancytopenia, Lung Adenocarcinoma Metastatic, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Glucophage
    Administration route: Oral
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2004-11-01

Imodium
    Start date: 2006-01-01

Lytos

Alimta
    Indication: Metastatic Bronchial Carcinoma
    Start date: 2007-02-01
    End date: 2007-02-22

Tarceva
    Start date: 2006-01-01
    End date: 2007-04-01

Micardis
    Administration route: Oral
    Start date: 2005-12-01

Other drugs received by patient: Aluminum Hydroxide and Magnesium Trisilicate; Granocyte; Neorecormon; Folic Acid; Vitamin B-12



Adverse event in female receiving Imodium (Loperamide)

Reported by a health professional (non-physician/pharmacist) from Taiwan, Province of China on 2007-05-14

Patient: female

Adverse reactions / side effects: Flushing

Adverse event resulted in: disablity

Suspect drug(s):
Imodium
    Administration route: Oral
    Indication: Diarrhoea

Imodium
    Administration route: Oral

Butylscopolamine
    Indication: Gastrointestinal Pain

Other drugs received by patient: Panadol; Coliopan; Baluna; Novamin



Adverse event in 50 year old male receiving Imodium (Loperamide)

Reported by a health professional (non-physician/pharmacist) from France on 2007-05-11

Patient: 50 year old male

Adverse reactions / side effects: Faecaloma

Adverse event resulted in: hospitalization

Suspect drug(s):
Imodium
    Administration route: Oral
    Indication: Diarrhoea

Aluminum Hydroxide and Magnesium Trisilicate
    Administration route: Oral
    Indication: Diarrhoea

Tiorfan
    Administration route: Oral
    Indication: Diarrhoea

Other drugs received by patient: Zyprexa; Dafalgan; Dantrium



Adverse event in 15 year old male receiving Imodium (Loperamide)

Reported by a physician from Austria on 2007-04-18

Patient: 15 year old male

Adverse reactions / side effects: Paraesthesia

Suspect drug(s):
Imodium (Loperamide)



Adverse event in 15 year old male receiving Imodium (Loperamide)

Reported by a physician from Austria on 2007-04-12

Patient: 15 year old male

Adverse reactions / side effects: Paraesthesia

Suspect drug(s):
Imodium (Loperamide)



Adverse event in female receiving Imodium (Loperamide)

Reported by a health professional (non-physician/pharmacist) from Taiwan, Province of China on 2007-04-11

Patient: female

Adverse reactions / side effects: Flushing

Adverse event resulted in: disablity

Suspect drug(s):
Imodium
    Indication: Diarrhoea

Imodium

Butylscopolamine
    Indication: Gastrointestinal Pain



Adverse event in 19 year old male receiving Imodium (Loperamide)

Reported by a pharmacist from Germany on 2007-04-06

Patient: 19 year old male

Adverse reactions / side effects: Drug Abuser

Suspect drug(s):
Lopedium Akut BEI Akutem Durchfall (Ngx)(loperamide) Capsule, 2MG
    Dosage: oral
    Administration route: Oral

Imodium



Adverse event in female receiving Imodium (Loperamide)

Reported by a health professional (non-physician/pharmacist) from Taiwan, Province of China on 2007-04-06

Patient: female

Adverse reactions / side effects: Flushing

Adverse event resulted in: disablity

Suspect drug(s):
Imodium
    Indication: Diarrhoea

Imodium

Butylscopolamine
    Indication: Gastrointestinal Pain

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