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Metronidazole (Metronidazole) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Metronidazole. 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 side effect / 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 (151)
     Nausea (14)International Normalised Ratio Increased (13)Drug Interaction (12)more >>

Cases resulting in a serious event (147)
     Nausea (14)International Normalised Ratio Increased (13)Drug Interaction (12)more >>

Cases resulting in death (14)
     Metabolic Acidosis (5)Myocardial Infarction (5)Disorientation (4)more >>

Cases resulting in life threatening events (12)
     Anaemia (3)Neutropenia (3)Dyspnoea (2)more >>

Cases resulting in hospitalization (75)
     Nausea (8)International Normalised Ratio Increased (7)Confusional State (6)more >>

Cases resulting in disability (13)
     Clonus (5)Urinary Incontinence (5)Eye Rolling (5)more >>

Cases resulting in other serious reactions (71)
     Drug Interaction (9)Coordination Abnormal (8)Nausea (7)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Metronidazole. For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in 54 year old male receiving Metronidazole

Reported by a individual with unspecified qualification on 2007-10-31

Patient: 54 year old male, weighing 80.0 kg (176.0 pounds)

Adverse reactions / side effects: Mania, Circadian Rhythm Sleep Disorder, Lethargy

Adverse event resulted in: hospitalization

Suspect drug(s):
Metronidazole

Other drugs received by patient: Amoxicillin; Garlic Extract



Adverse event in 38 year old female receiving Metronidazole

Reported by a individual with unspecified qualification from Netherlands on 2007-10-31

Patient: 38 year old female

Adverse reactions / side effects: Encephalopathy

Adverse event resulted in: death

Suspect drug(s):
Metronidazole
    Indication: Wound Infection

Metronidazole

Metronidazole
    Indication: Osteomyelitis

Metronidazole

Haloran / 00372302 /

Other drugs received by patient: Vancomycin; Teicoplanin



Adverse event in female receiving Metronidazole

Reported by a individual with unspecified qualification on 2007-10-18

Patient: female

Adverse reactions / side effects: Premature Baby

Suspect drug(s):
Paracetamol

Morphine

Dexamethasone 0.5mg TAB
    Indication: Maternal Therapy TO Enhance Foetal Lung Maturity

Chlorpheniramine TAB

Cyclosporine

Gentamicin

Metronidazole

Compound Sodium Lactate



Adverse event in 30 year old female receiving Metronidazole

Reported by a individual with unspecified qualification on 2007-10-18

Patient: 30 year old female, weighing 72.0 kg (158.4 pounds)

Adverse reactions / side effects: Face Oedema, Psoriasis, Pyrexia, Somnolence, Generalised Oedema

Suspect drug(s):
Paracetamol
    Indication: Pain

Morphine
    Administration route: Oral
    Indication: Pain

Chlorpheniramine TAB
    Indication: Pruritus

Gentamicin

Metronidazole

Other drugs received by patient: Dexamethasone 0.5mg TAB; Cyclosporine; Compound Sodium Lactate



Adverse event in 36 year old female receiving Metronidazole

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-16

Patient: 36 year old female

Adverse reactions / side effects: Swelling Face, Obstructive Airways Disorder

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Metronidazole
    Dosage: 1200 mg (400 mg, 3 in 1 d) oral; 1200 mg (400 mg, 3 in 1 d) oral
    Administration route: Oral
    Indication: Infection
    Start date: 2007-08-10
    End date: 2007-08-14

Metronidazole
    Dosage: 1200 mg (400 mg, 3 in 1 d) oral; 1200 mg (400 mg, 3 in 1 d) oral
    Administration route: Oral
    Indication: Infection
    Start date: 2007-07-25



Adverse event in 58 year old female receiving Metronidazole

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-16

Patient: 58 year old female

Adverse reactions / side effects: Electrocardiogram T Wave Amplitude Decreased, Chills, Headache, Pyrexia, Haematocrit Decreased, Fibrin D Dimer Increased, Chest Pain, Blood Creatinine Increased, Lethargy, Blood Urea Increased, Vomiting, Nausea, Haematuria, Thrombotic Thrombocytopenic Purpura, Haemoglobin Decreased, Troponin I Increased, Asthenia

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Metronidazole

Other drugs received by patient: Sertraline; Quetiapine Fumarate; Lorazepam; Zolpidem Tartrate



Adverse event in 43 year old female receiving Metronidazole

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-15

Patient: 43 year old female, weighing 60.0 kg (132.0 pounds)

Adverse reactions / side effects: Stomach Discomfort, Headache, Tongue Coated, Dysgeusia, Fatigue, Malaise, Diarrhoea, Dizziness, Asthenia, Feeling Abnormal

Suspect drug(s):
Metronidazole



Adverse event in 36 year old female receiving Metronidazole

Reported by a individual with unspecified qualification from United States on 2007-10-15

Patient: 36 year old female

Adverse reactions / side effects: Swelling Face, Obstructive Airways Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Metronidazole
    Dosage: 400 mg, tid
    Indication: Infection
    Start date: 2007-08-10
    End date: 2007-08-14

Metronidazole
    Dosage: 400 mg, tid
    Indication: Infection
    Start date: 2007-07-25



Adverse event in 36 year old female receiving Metronidazole

Reported by a individual with unspecified qualification on 2007-10-09

Patient: 36 year old female

Adverse reactions / side effects: Swelling Face, Obstructive Airways Disorder

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Metronidazole
    Administration route: Oral
    Indication: Infection
    Start date: 2007-08-10
    End date: 2007-08-14

Metronidazole
    Administration route: Oral
    Start date: 2007-07-25



Adverse event in 67 year old female receiving Metronidazole

Reported by a physician from NEW Zealand on 2007-10-09

Patient: 67 year old female

Adverse reactions / side effects: Colour Vision Tests Abnormal, Optic Atrophy, Pain in Extremity, Visual Acuity Reduced, Muscular Weakness, Sensory Loss, Peripheral Sensory Neuropathy, Optic Neuropathy, Gastrointestinal Disorder, Gait Disturbance

Suspect drug(s):
Metronidazole



Adverse event in 43 year old female receiving Metronidazole

Reported by a individual with unspecified qualification on 2007-10-09

Patient: 43 year old female, weighing 60.0 kg (132.0 pounds)

Adverse reactions / side effects: Stomach Discomfort, Headache, Tongue Coated, Dysgeusia, Fatigue, Malaise, Diarrhoea, Dizziness, Asthenia, Feeling Abnormal

Suspect drug(s):
Metronidazole



Adverse event in male receiving Metronidazole

Reported by a physician from United States on 2007-10-09

Patient: male, weighing 99.0 kg (217.8 pounds)

Adverse reactions / side effects: Acid Base Balance Abnormal

Adverse event resulted in: hospitalization

Suspect drug(s):
Ceftriaxone
    Dosage: 2 g daily
    Indication: Appendicitis
    Start date: 2007-09-24
    End date: 2007-09-27

Metronidazole
    Dosage: 500 mg daily
    Indication: Appendicitis
    Start date: 2007-09-24
    End date: 2007-09-27



Adverse event in 53 year old male receiving Metronidazole

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-05

Patient: 53 year old male

Adverse reactions / side effects: Metabolic Acidosis, Aminoaciduria, Myocardial Infarction

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Paracetamol

Paracetamol
    Indication: Analgesia

Levofloxacin
    Indication: Sepsis

Augmentin '125'
    Indication: Sepsis

Gentamicin
    Indication: Sepsis

Metronidazole
    Indication: Sepsis

TPN
    Indication: Parenteral Nutrition

Vancomycin
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Diclofenac Sodium; Omeprazole; Metoclopramide



Adverse event in 67 year old female receiving Metronidazole

Reported by a physician from NEW Zealand on 2007-10-05

Patient: 67 year old female

Adverse reactions / side effects: Optic Atrophy, Colour Vision Tests Abnormal, Pain in Extremity, Visual Acuity Reduced, Muscular Weakness, Peripheral Sensory Neuropathy, Optic Neuropathy, NO Therapeutic Response, Gait Disturbance

Suspect drug(s):
Metronidazole



Adverse event in 53 year old male receiving Metronidazole

Reported by a consumer/non-health professional from United Kingdom on 2007-10-04

Patient: 53 year old male

Adverse reactions / side effects: Fistula, Metabolic Acidosis, Disorientation, Myocardial Infarction

Adverse event resulted in: death

Suspect drug(s):
Augmentin '125'

Paracetamol
    Administration route: Oral

Gentamicin

Levofloxacin

Metronidazole

Vancomycin

Other drugs received by patient: Diclofenac Sodium; Metoclopramide; Omeprazole



Adverse event in 53 year old male receiving Metronidazole

Reported by a consumer/non-health professional from United Kingdom on 2007-10-04

Patient: 53 year old male

Adverse reactions / side effects: Fistula, Metabolic Acidosis, Disorientation, Myocardial Infarction

Adverse event resulted in: death

Suspect drug(s):
Augmentin '125'
    Indication: Drug USE FOR Unknown Indication

Gentamicin
    Indication: Drug USE FOR Unknown Indication

Levofloxacin
    Indication: Drug USE FOR Unknown Indication

Metronidazole
    Indication: Drug USE FOR Unknown Indication

Paracetamol
    Administration route: Oral

Vancomycin
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Diclofenac Sodium; Metoclopramide; Omeprazole



Adverse event in 53 year old male receiving Metronidazole

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-02

Patient: 53 year old male

Adverse reactions / side effects: Metabolic Acidosis, General Physical Health Deterioration, Disorientation, Urine Amino Acid Level Increased, Myocardial Infarction

Adverse event resulted in: death

Suspect drug(s):
Metronidazole
    Indication: Analgesia

Metronidazole
    Indication: Infection

Augmentin '125'
    Indication: Infection

Levofloxacin
    Indication: Infection

Gentamicin
    Indication: Infection

Acetaminophen
    Indication: Analgesia

Acetaminophen
    Indication: Infection

Vancomycin
    Indication: Infection

Diclofenac Sodium
    Indication: Analgesia

Metoclopramide

Omeprazole



Adverse event in 45 year old female receiving Metronidazole

Reported by a individual with unspecified qualification from United States on 2007-10-01

Patient: 45 year old female, weighing 77.1 kg (169.6 pounds)

Adverse reactions / side effects: Abdominal Pain, Fatigue, Nausea, Haemorrhoids, Anger, Clostridium Difficile Colitis

Suspect drug(s):
Cipro
    Dosage: 500 mg, total daily, oral
    Administration route: Oral
    Indication: Diverticulitis
    Start date: 2007-01-28

Metronidazole
    Indication: Diverticulitis



Adverse event in 84 year old female receiving Metronidazole

Reported by a individual with unspecified qualification on 2007-10-01

Patient: 84 year old female, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Pancreatitis Acute

Adverse event resulted in: death

Suspect drug(s):
Metronidazole

Other drugs received by patient: Alfacalcidol; Aspirin; Calcichew / 00108001 /; Clopidogrel; Flucloxacillin; Glyceryl Trinitrate; Hydroxyzine; Ismn; Lansoprazole; Naloxone; Paracetamol



Adverse event in 69 year old male receiving Metronidazole

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-01

Patient: 69 year old male

Adverse reactions / side effects: Hypoaesthesia, Gait Disturbance, Cerebrovascular Accident

Adverse event resulted in: hospitalization

Suspect drug(s):
Metronidazole



Adverse event in 53 year old male receiving Metronidazole

Reported by a individual with unspecified qualification on 2007-10-01

Patient: 53 year old male

Adverse reactions / side effects: Metabolic Acidosis, General Physical Health Deterioration, Disorientation, Myocardial Infarction

Adverse event resulted in: death

Suspect drug(s):
Augmentin (Formulation Unknown) (Amo. Trihyd+pot.clavulan.)

Acetaminophen
    Dosage: oral
    Administration route: Oral
    Indication: Analgesia

Gentamicin Sulfate

Levofloxacin

Metronidazole

Vancomycin

Other drugs received by patient: Diclofenac Sodium; Metoclopramide; Omeprazole



Adverse event in 50 year old male receiving Metronidazole

Reported by a physician from Germany on 2007-07-30

Patient: 50 year old male, weighing 72.0 kg (158.4 pounds)

Adverse reactions / side effects: Abdominal Pain, Peritoneal Lavage, Laparotomy, Adhesiolysis, Intestinal Haemorrhage, Ileus, Large Intestinal Ulcer, Large Intestinal Ulcer Haemorrhage, Colitis, Abscess, Splenectomy, Colectomy, Splenic Rupture, Infection

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Mycophenolate Mofetil
    Dosage: 1 mg, bid
    Administration route: Oral
    Indication: Heart Transplant
    Start date: 2007-05-28
    End date: 2007-06-12

Mycophenolate Mofetil
    Dosage: 1mg daily
    Administration route: Oral
    Start date: 2007-06-30
    End date: 2007-07-21

Decortin-H
    Dosage: 42.5 mg, bid
    Administration route: Oral
    Indication: Heart Transplant
    Start date: 2007-05-27

Tazobac
    Dosage: 4500 mg, bid
    Indication: Bronchitis
    Start date: 2007-05-29
    End date: 2007-06-05

Vancomycin

Metronidazole

Neoral
    Dosage: 325 mg, bid
    Administration route: Oral
    Indication: Heart Transplant
    Start date: 2007-05-26



Adverse event in 58 year old female receiving Metronidazole

Reported by a individual with unspecified qualification from United States on 2007-07-30

Patient: 58 year old female

Adverse reactions / side effects: Vomiting, Nausea, Chest Pain, Haematuria, Chills, Pyrexia, Headache, Thrombotic Thrombocytopenic Purpura, Asthenia, Lethargy

Adverse event resulted in: hospitalization

Suspect drug(s):
Metronidazole

Other drugs received by patient: Sertraline; Quetiapine Fumarate; Lorazepam; Zolpidem Tartrate



Adverse event in 62 year old male receiving Metronidazole

Reported by a pharmacist from United States on 2007-07-30

Patient: 62 year old male

Adverse reactions / side effects: International Normalised Ratio Increased

Adverse event resulted in: life threatening event

Suspect drug(s):
Warfarin Sodium
    Dosage: 2mg every day po
    Administration route: Oral
    Indication: Deep Vein Thrombosis
    Start date: 2007-05-23
    End date: 2007-06-18

Metronidazole
    Dosage: 500mg tid po
    Administration route: Oral
    Start date: 2007-06-16
    End date: 2007-06-18



Adverse event in male receiving Metronidazole

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-24

Patient: male

Adverse reactions / side effects: Mania

Suspect drug(s):
Metronidazole
    Indication: Drug USE FOR Unknown Indication

Sulfasalazine
    Indication: Drug USE FOR Unknown Indication

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