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Lamisil (Terbinafine) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Lamisil (Terbinafine). 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 (291)
     Drug Interaction (24)Alanine Aminotransferase Increased (21)Liver Disorder (21)more >>

Cases resulting in a serious event (287)
     Drug Interaction (24)Alanine Aminotransferase Increased (21)Liver Disorder (21)more >>

Cases resulting in death (12)
     Drug Interaction (9)Jaundice (7)Liver Disorder (7)more >>

Cases resulting in life threatening events (23)
     Drug Interaction (15)Liver Disorder (9)Jaundice (8)more >>

Cases resulting in hospitalization (85)
     Drug Interaction (17)Liver Disorder (14)Jaundice (13)more >>

Cases resulting in disability (10)
     Haematuria (3)Malaise (3)Gastrointestinal Disorder (3)more >>

Cases resulting in other serious reactions (210)
     Blood Creatine Phosphokinase Increased (17)Nausea (17)Alanine Aminotransferase Increased (17)more >>

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

Adverse event in 69 year old male receiving Lamisil (Terbinafine)

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

Patient: 69 year old male

Adverse reactions / side effects: Hallucination, Visual, Drug Interaction

Suspect drug(s):
Comtess
    Dosage: 800 mg/day
    Indication: Parkinson's Disease
    Start date: 2004-01-01

Lamisil
    Dosage: 205 mg/day
    Administration route: Oral
    Indication: Nail Tinea
    Start date: 2007-06-29

Requip
    Dosage: 21 mg/day
    Indication: Parkinson's Disease
    Start date: 2004-01-01

Sinemet
    Dosage: 400 mg/day
    Indication: Parkinson's Disease
    Start date: 2004-01-01

Other drugs received by patient: Marevan; Nitroglycerin; Verruxin



Adverse event in 34 year old female receiving Lamisil (Terbinafine)

Reported by a pharmacist from Japan on 2007-10-30

Patient: 34 year old female, weighing 58.0 kg (127.6 pounds)

Adverse reactions / side effects: Surgery, Drug Exposure During Pregnancy, Intra-Uterine Death, Abortion Missed, Genital Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 54 year old female receiving Lamisil (Terbinafine)

Reported by a physician from Japan on 2007-10-29

Patient: 54 year old female

Adverse reactions / side effects: Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Blood Cholinesterase Increased

Suspect drug(s):
Lamisil
    Dosage: 125 mg/d
    Administration route: Oral
    Indication: Nail Tinea
    Start date: 2007-05-23
    End date: 2007-10-13

Lendormin
    Administration route: Oral
    Start date: 2007-09-10
    End date: 2007-10-15



Adverse event in 69 year old male receiving Lamisil (Terbinafine)

Reported by a individual with unspecified qualification from Finland on 2007-10-29

Patient: 69 year old male

Adverse reactions / side effects: Nail Tinea, Hallucination, Visual, Drug Interaction

Suspect drug(s):
Entacapone
    Dosage: 800 mg
    Indication: Parkinson's Disease
    Start date: 2004-01-01

Lamisil
    Dosage: 205 mg oral
    Administration route: Oral
    Indication: Nail Tinea
    Start date: 2007-06-29

Requip
    Dosage: 21 mg
    Indication: Parkinson's Disease
    Start date: 2004-01-01

Sinemet
    Dosage: 400 mg
    Indication: Parkinson's Disease
    Start date: 2004-01-01

Other drugs received by patient: Marevan; Nitroglycerin; Veruxin



Adverse event in 60 year old male receiving Lamisil (Terbinafine)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-26

Patient: 60 year old male, weighing 83.4 kg (183.6 pounds)

Adverse reactions / side effects: Headache, Throat Tightness

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 77 year old male receiving Lamisil (Terbinafine)

Reported by a physician from United Kingdom on 2007-10-26

Patient: 77 year old male

Adverse reactions / side effects: Drug Ineffective, Condition Aggravated, Tinea Pedis

Adverse event resulted in: death

Suspect drug(s):
Lamisil (Terbinafine)

Other drugs received by patient: Aspirin; Atenolol; Bizinjection



Adverse event in 49 year old female receiving Lamisil (Terbinafine)

Reported by a consumer/non-health professional from Mexico on 2007-10-26

Patient: 49 year old female

Adverse reactions / side effects: Drug Interaction, Tremor

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 72 year old female receiving Lamisil (Terbinafine)

Reported by a pharmacist from Japan on 2007-10-24

Patient: 72 year old female

Adverse reactions / side effects: Dyspnoea, Sputum Retention

Suspect drug(s):
Lamisil (Terbinafine)

Other drugs received by patient: Tagamet



Adverse event in 26 year old male receiving Lamisil (Terbinafine)

Reported by a physician from France on 2007-10-24

Patient: 26 year old male, weighing 120.0 kg (264.0 pounds)

Adverse reactions / side effects: Facial Palsy, Hemiparesis

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in male receiving Lamisil (Terbinafine)

Reported by a consumer/non-health professional from United States on 2007-10-24

Patient: male

Adverse reactions / side effects: Panic Attack

Suspect drug(s):
Lamisil (Terbinafine)

Other drugs received by patient: Vytorin; Diovan



Adverse event in male receiving Lamisil (Terbinafine)

Reported by a individual with unspecified qualification from United States on 2007-10-23

Patient: male

Adverse reactions / side effects: Retinal Haemorrhage

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in male receiving Lamisil (Terbinafine)

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

Patient: male

Adverse reactions / side effects: Rash Pustular, Pruritus, Oedema Peripheral

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in receiving Lamisil (Terbinafine)

Reported by a pharmacist from Denmark on 2007-10-23

Patient:

Adverse reactions / side effects: Haemorrhage, Rash, Scar

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 58 year old female receiving Lamisil (Terbinafine)

Reported by a physician from United States on 2007-10-19

Patient: 58 year old female

Adverse reactions / side effects: Weight Decreased, Drug Toxicity, Liver Injury, Hepatotoxicity, Cholestasis, Hepatitis, Liver Disorder

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 58 year old male receiving Lamisil (Terbinafine)

Reported by a physician from United States on 2007-10-16

Patient: 58 year old male

Adverse reactions / side effects: Pancreatitis Acute, Abdominal Pain, Jaundice, Bile Duct Obstruction, Pruritus, Liver Disorder, Pancreatic Disorder, Hepatobiliary Disease, Bile Duct Stenosis, Biliary Drainage, Urine Colour Abnormal, Alcoholic Pancreatitis, Intestinal Functional Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Lamisil (Terbinafine)

Other drugs received by patient: Benicar; Norvasc; Probenecid; Zetia; Prevacid



Adverse event in 41 year old male receiving Lamisil (Terbinafine)

Reported by a physician from United States on 2007-10-16

Patient: 41 year old male, weighing 131.5 kg (289.4 pounds)

Adverse reactions / side effects: Rhabdomyolysis, Diarrhoea, Renal Failure Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Aripiprazole
    Dosage: 30mg daily po
    Administration route: Oral
    Indication: Schizophrenia, Paranoid Type
    Start date: 2006-01-01
    End date: 2007-02-01

Lamisil
    Indication: Onychomycosis
    Start date: 2007-01-01
    End date: 2007-02-01



Adverse event in male receiving Lamisil (Terbinafine)

Reported by a health professional (non-physician/pharmacist) from France on 2007-10-15

Patient: male

Adverse reactions / side effects: Cutaneous Vasculitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Advil Liqui-Gels
    Dosage: unknown
    Administration route: Oral
    Start date: 2006-09-22
    End date: 2006-09-26

Colchicine
    Dosage: unknown
    Administration route: Oral
    Start date: 2006-10-05
    End date: 2006-10-07

Lamisil
    Dosage: unknown
    Administration route: Oral
    Start date: 2006-09-26
    End date: 2006-10-07

Zithromax
    Dosage: unknown
    Administration route: Oral
    Start date: 2006-09-22
    End date: 2006-09-26



Adverse event in 25 year old female receiving Lamisil (Terbinafine)

Reported by a physician from Japan on 2007-10-15

Patient: 25 year old female

Adverse reactions / side effects: Drug Exposure During Pregnancy, Abortion Induced

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 70 year old male receiving Lamisil (Terbinafine)

Reported by a consumer/non-health professional from United Kingdom on 2007-10-15

Patient: 70 year old male

Adverse reactions / side effects: Localised Infection, Cellulitis, Disease Recurrence, Pain in Extremity, Oedema Peripheral, Erythema, Tinea Pedis, Influenza Like Illness

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 57 year old female receiving Lamisil (Terbinafine)

Reported by a consumer/non-health professional from Australia on 2007-10-15

Patient: 57 year old female

Adverse reactions / side effects: Hepatic Pain, Self Esteem Decreased, Depression Suicidal, Sensitivity of Teeth, Crying, Aggression

Suspect drug(s):
Lamisil (Terbinafine)

Other drugs received by patient: Vitamins



Adverse event in 31 year old male receiving Lamisil (Terbinafine)

Reported by a physician from France on 2007-10-12

Patient: 31 year old male, weighing 95.0 kg (209.0 pounds)

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Muscle Spasms

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 53 year old male receiving Lamisil (Terbinafine)

Reported by a individual with unspecified qualification from France on 2007-10-12

Patient: 53 year old male

Adverse reactions / side effects: Cutaneous Vasculitis, Vascular Purpura

Adverse event resulted in: hospitalization

Suspect drug(s):
Advil Liqui-Gels
    Administration route: Oral
    Start date: 2006-09-22
    End date: 2006-09-26

Colchicine
    Administration route: Oral
    Start date: 2006-10-05
    End date: 2006-10-07

Lamisil
    Administration route: Oral
    Start date: 2006-09-26
    End date: 2006-10-07

Zithromax
    Administration route: Oral
    Start date: 2006-09-22
    End date: 2006-09-26



Adverse event in male receiving Lamisil (Terbinafine)

Reported by a consumer/non-health professional from United Kingdom on 2007-10-09

Patient: male

Adverse reactions / side effects: Fatigue, Asthenia, Depressed Mood

Suspect drug(s):
Lamisil (Terbinafine)

Other drugs received by patient: Olanzapine



Adverse event in male receiving Lamisil (Terbinafine)

Reported by a consumer/non-health professional from Australia on 2007-10-09

Patient: male

Adverse reactions / side effects: Inappropriate Schedule of Drug Administration, Cellulitis, Drug Ineffective

Suspect drug(s):
Lamisil (Terbinafine)



Adverse event in 50 year old female receiving Lamisil (Terbinafine)

Reported by a consumer/non-health professional from Philippines on 2007-10-08

Patient: 50 year old female, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Syncope, Headache, Hypertension

Adverse event resulted in: life threatening event

Suspect drug(s):
Lamisil (Terbinafine)

Other drugs received by patient: Centrum; Nutricap; Vitamin B Complex CAP; Ascorbic Acid

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