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Prevacid (Lansoprazole) - Adverse Event Reports - Other Serious Reactions

 



Index of reports > Cases resulting in other serious reactions (13)

     Nausea (5)Blood Pressure Inadequately Controlled (4)Urticaria (3)Diarrhoea (3)Dizziness (3)Hiatus Hernia (2)Auricular Swelling (2)Arthralgia (2)Sepsis (2)Pneumonitis (2)

Below is the selection of adverse event reports related to Prevacid (Lansoprazole) that includes cases resulting in other serious reactions.

Adverse event in 2 year old male receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-10-29

Patient: 2 year old male

Adverse reactions / side effects: Anaphylactic Reaction

Suspect drug(s):
Miralax
    Dosage: po
    Administration route: Oral
    Indication: Constipation
    Start date: 2006-06-01
    End date: 2007-10-17

Prevacid
    Indication: Drug USE FOR Unknown Indication

Allegra
    Indication: Drug USE FOR Unknown Indication

Pulmicort
    Indication: Drug USE FOR Unknown Indication

Singulair
    Indication: Drug USE FOR Unknown Indication

Neocate
    Indication: Drug USE FOR Unknown Indication



Adverse event in 3 year old female receiving Prevacid (Lansoprazole)

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

Patient: 3 year old female, weighing 22.7 kg (49.9 pounds)

Adverse reactions / side effects: Dermatitis Allergic, LIP Swelling, Skin Chapped, Aspiration Bone Marrow Abnormal, Skin Exfoliation, Urticaria, Respiratory Syncytial Virus Infection, Helicobacter Sepsis, Auricular Swelling, Blood Pressure Inadequately Controlled, Bacterial Sepsis, Skin Haemorrhage, Angioedema, Swelling Face, Drug Hypersensitivity, Staphylococcal Sepsis, Sepsis, Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Amlodipine Besylate
    Dosage: daily;oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-04-01

Amlodipine Besylate
    Dosage: daily;oral
    Administration route: Oral
    Indication: Secondary Hypertension
    Start date: 2004-04-01

Enalapril Maleate
    Indication: Hypertension
    Start date: 2004-05-01
    End date: 2006-06-01

Enalapril Maleate
    Indication: Secondary Hypertension
    Start date: 2004-05-01
    End date: 2006-06-01

Enalapril Maleate
    Indication: Hypertension
    Start date: 2007-09-07
    End date: 2007-10-02

Enalapril Maleate
    Indication: Secondary Hypertension
    Start date: 2007-09-07
    End date: 2007-10-02

Enalapril Maleate
    Dosage: daily;oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-05-01
    End date: 2006-06-01

Enalapril Maleate
    Dosage: daily;oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-09-07
    End date: 2007-10-02

Prevacid
    Start date: 2004-01-01
    End date: 2006-06-01

Diflucan
    Dosage: oral
    Administration route: Oral
    Indication: Fungal Infection
    Start date: 2007-08-29
    End date: 2007-09-25

Other drugs received by patient: Prednisolone; Cyclosporine; Cozaar



Adverse event in 3 year old female receiving Prevacid (Lansoprazole)

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

Patient: 3 year old female, weighing 22.7 kg (49.9 pounds)

Adverse reactions / side effects: LIP Swelling, Dermatitis Allergic, Graft Versus Host Disease, Skin Exfoliation, Urticaria, Skin Fissures, Respiratory Syncytial Virus Infection, Helicobacter Sepsis, Dermatitis Contact, Bone Marrow Disorder, Auricular Swelling, Blood Pressure Inadequately Controlled, Bacterial Infection, Bacterial Sepsis, Skin Haemorrhage, Swelling Face, Dermatitis Atopic, Drug Hypersensitivity, Ill-Defined Disorder, Staphylococcal Sepsis, Bacteraemia, Sepsis, NO Therapeutic Response, Neutropenia, Inflammation

Adverse event resulted in: hospitalization

Suspect drug(s):
Enalapril Maleate
    Dosage: 1 tablet, daily, oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-04-30
    End date: 2006-06-01

Enalapril Maleate
    Dosage: 1 tablet, daily, oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-09-07
    End date: 2007-10-02

Enalapril Maleate
    Dosage: 1 tablet , daily, (alt w/ watson),oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-04-30
    End date: 2006-06-01

Enalapril Maleate
    Dosage: 1 tablet , daily, (alt w/ watson),oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-09-07
    End date: 2007-10-02

Amlodipine
    Dosage: oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-04-30
    End date: 2007-10-02

Prevacid
    Start date: 2004-01-01
    End date: 2006-06-01

Diflucan
    Dosage: oral
    Administration route: Oral
    Indication: Fungal Infection
    Start date: 2007-08-29
    End date: 2007-09-25

Other drugs received by patient: Prednisolone; Closporine (Ciclosporin)



Adverse event in 67 year old male receiving Prevacid (Lansoprazole)

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

Patient: 67 year old male, weighing 140.9 kg (310.0 pounds)

Adverse reactions / side effects: Blood Glucose Increased

Suspect drug(s):
Toprol-XL
    Administration route: Oral
    Indication: Cardiac Disorder

Prevacid
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2004-01-01

Zocor
    Administration route: Oral
    Indication: Blood Cholesterol Increased

Hyzaar
    Administration route: Oral
    Indication: Hypertension

Enalapril Maleate
    Administration route: Oral
    Indication: Hypertension

Diltiazem
    Administration route: Oral
    Indication: Hypertension

Aspirin
    Administration route: Oral
    Indication: Cardiac Disorder

Aspirin
    Administration route: Oral
    Indication: Headache



Adverse event in female receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-06-01

Patient: female

Adverse reactions / side effects: Malabsorption, Muscle Atrophy, Pneumonia, Psychomotor Hyperactivity, Drug Ineffective, Nausea, Crohn's Disease, Anxiety, Fatigue, Insomnia, Bone Disorder, Gastrooesophageal Reflux Disease

Adverse event resulted in: hospitalization

Suspect drug(s):
Prednisone TAB
    Indication: Crohn's Disease

Chantix
    Indication: EX-Smoker

Zithromax
    Indication: Pneumonia
    Start date: 2007-01-01
    End date: 2007-01-01

Amoxicillin
    Indication: Pneumonia

Drug, Unspecified

Prevacid
    Indication: Gastrooesophageal Reflux Disease

Prilosec
    Indication: Gastrooesophageal Reflux Disease

Acetylsalicylic Acid SRT
    Indication: Cardiovascular Event Prophylaxis

Other drugs received by patient: Drug, Unspecified; Asacol; Prilosec; Acetylsalicylic Acid SRT



Adverse event in female receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from United States on 2007-05-31

Patient: female

Adverse reactions / side effects: Breast Cancer, Maculopathy

Suspect drug(s):
Prevacid (Lansoprazole)



Adverse event in female receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-05-29

Patient: female, weighing 22.7 kg (49.9 pounds)

Adverse reactions / side effects: Dermatitis

Suspect drug(s):
Vistaril (Oral Susp)
    Indication: Hypersensitivity

Zyrtec
    Indication: Hypersensitivity

Fluconazole

Zyvox Suspension, Oral
    Indication: Staphylococcal Infection
    Start date: 2007-05-01
    End date: 2007-05-20

Amlodipine

Acyclovir

Calcium Chloride

Creon

Daclizumab

Enalapril Maleate

Hydramine

Levaquin
    Start date: 2007-01-01
    End date: 2007-05-01

Mupirocin

Neutra-Phos

Orapred

Pentamidine Isethionate

Prednisone TAB

Prevacid

Protopic

ALL Other Therapeutic Products

Vitamin D

Zantac

Flintstones Multiple Vitamins

Cyclosporine

Magnesium Sulfate



Adverse event in female receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-05-18

Patient: female

Adverse reactions / side effects: Malabsorption, Muscle Atrophy, Pneumonia, Psychomotor Hyperactivity, Drug Ineffective, Nausea, Crohn's Disease, Anxiety, Fatigue, Insomnia, Bone Disorder, Gastrooesophageal Reflux Disease

Adverse event resulted in: hospitalization

Suspect drug(s):
Prednisone TAB
    Indication: Crohn's Disease

Chantix
    Indication: EX-Smoker

Zithromax
    Indication: Pneumonia
    Start date: 2007-01-01
    End date: 2007-01-01

Amoxicillin
    Indication: Pneumonia

Drug, Unspecified

Prevacid
    Indication: Gastrooesophageal Reflux Disease

Prilosec
    Indication: Gastrooesophageal Reflux Disease

Acetylsalicylic Acid SRT
    Indication: Cardiovascular Event Prophylaxis

Other drugs received by patient: Drug, Unspecified; Asacol



Adverse event in 47 year old male receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-03-05

Patient: 47 year old male, weighing 89.4 kg (196.6 pounds)

Adverse reactions / side effects: Weight Decreased, Diarrhoea, Food Poisoning

Suspect drug(s):
Prevacid (Lansoprazole)



Adverse event in 12 year old female receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-02-20

Patient: 12 year old female

Adverse reactions / side effects: Colour Blindness, Dizziness, Blindness, Loss of Consciousness

Suspect drug(s):
Zantac
    Dosage: 150mg per day
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2006-05-22
    End date: 2006-06-08

Prevacid
    Dosage: 30mg per day
    Start date: 2006-05-22
    End date: 2006-06-08

Other drugs received by patient: NO Concurrent Medication



Adverse event in female receiving Prevacid (Lansoprazole)

Reported by a lawyer from United States on 2007-02-14

Patient: female, weighing 85.7 kg (188.5 pounds)

Adverse reactions / side effects: Agitation, Abdominal Pain, Pruritus, Sciatica, Headache, Erythema, Delusion, Duodenitis, Oesophagitis, Uterine Leiomyoma, Blood Pressure Inadequately Controlled, Pneumonitis, Back Pain, Chest Discomfort, Hiatus Hernia, Pain in Extremity, Hyperglycaemia, Coronary Artery Disease, Hypoaesthesia, Dehydration, Disorientation, Myalgia, Chest Pain, Dizziness, Intestinal Polyp, Vomiting, Viral Infection, Nausea, Musculoskeletal Pain, Rash, Purpura, Facial Pain, Hypertensive Crisis, Limb Discomfort, Diarrhoea, Arthralgia, Pollakiuria, Gastroenteritis, Bronchitis, Infection

Adverse event resulted in: hospitalization

Suspect drug(s):
Procardia XL
    Administration route: Oral
    Indication: Hypertension

Procardia XL
    Administration route: Oral
    Start date: 2001-01-22
    End date: 2001-02-04

Procardia XL
    Administration route: Oral
    Start date: 2001-02-05
    End date: 2003-08-29

Nifedipine
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-02-01
    End date: 2004-01-01

Vasotec
    Start date: 1998-12-13
    End date: 1999-03-20

Cozaar
    Administration route: Oral
    Start date: 1999-12-07
    End date: 2001-01-22

Hyzaar
    Start date: 1999-12-07
    End date: 2000-01-01

Toprol-XL
    Start date: 1999-03-20

Paxil
    Start date: 1999-03-20

Clonidine
    Start date: 1999-03-20

Biaxin

Prilosec
    Start date: 2001-12-04
    End date: 2003-01-01

Premarin
    Start date: 2002-02-25

Diovane
    Start date: 2002-02-25
    End date: 2002-05-06

Benicar
    End date: 2003-08-29

Catapres
    Start date: 2001-01-22
    End date: 2001-01-01

Oxycodone
    Indication: Pain
    Start date: 2001-02-05

Lopressor
    Start date: 2001-01-01

Protonix
    Start date: 2001-01-01

Adalat
    Start date: 2001-02-05

Prevacid
    Start date: 2000-01-10

Nitrol
    Start date: 2002-05-06

Heparin
    Start date: 2002-05-06

Aspirin
    Start date: 2002-05-06

Vicodin ES



Adverse event in female receiving Prevacid (Lansoprazole)

Reported by a lawyer from United States on 2007-01-31

Patient: female, weighing 85.7 kg (188.5 pounds)

Adverse reactions / side effects: Abdominal Pain, Pruritus, Sciatica, Urticaria, Erythema, Delusion, Duodenitis, Oesophagitis, Uterine Leiomyoma, Blood Pressure Inadequately Controlled, Pneumonitis, Back Pain, Chest Discomfort, Hiatus Hernia, Pain in Extremity, Hyperglycaemia, Coronary Artery Disease, Hypoaesthesia, Dehydration, Chest Pain, Dizziness, Intestinal Polyp, Viral Infection, Vomiting, Nausea, Musculoskeletal Pain, Purpura, Facial Pain, Hypertensive Crisis, Limb Discomfort, Diarrhoea, Arthralgia, Gastroenteritis, Bronchitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Procardia XL
    Administration route: Oral
    Indication: Hypertension

Procardia XL
    Administration route: Oral
    Start date: 2001-01-22
    End date: 2001-02-04

Procardia XL
    Administration route: Oral
    Start date: 2001-02-05
    End date: 2003-08-29

Nifedipine
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-02-01
    End date: 2004-01-01

Vasotec
    Start date: 1998-12-13
    End date: 1999-03-20

Cozaar
    Administration route: Oral
    Start date: 1999-12-07
    End date: 2001-01-22

Hyzaar
    Start date: 1999-12-07
    End date: 2000-01-01

Toprol-XL
    Start date: 1999-03-20

Paxil
    Start date: 1999-03-20

Clonidine
    Start date: 1999-03-20

Biaxin

Prilosec
    Start date: 2001-12-04
    End date: 2003-01-01

Premarin
    Start date: 2002-02-25

Diovane
    Start date: 2002-02-25
    End date: 2002-05-06

Benicar
    End date: 2003-08-29

Catapres
    Start date: 2001-01-22
    End date: 2001-01-01

Oxycodone HCL
    Indication: Pain
    Start date: 2001-02-05

Lopressor
    Start date: 2001-01-01

Protonix
    Start date: 2001-01-01

Adalat
    Start date: 2001-02-05

Prevacid
    Start date: 2000-01-10

Nitrol
    Start date: 2002-05-06

Heparin
    Start date: 2002-05-06

Aspirin
    Start date: 2002-05-06

Vicodin ES



Adverse event in female receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-01-29

Patient: female, weighing 55.3 kg (121.7 pounds)

Adverse reactions / side effects: Gastrointestinal Haemorrhage, Peptic Ulcer, Nausea, Adverse Event, Melaena, Fall, Joint Injury

Suspect drug(s):
Chantix
    Administration route: Oral
    Indication: Smoking Cessation Therapy
    Start date: 2006-10-01
    End date: 2006-11-01

Aleve
    Indication: Musculoskeletal Pain

Protonix
    Indication: Peptic Ulcer

Nexium
    Indication: Peptic Ulcer

Prevacid
    Indication: Peptic Ulcer

Other drugs received by patient: Fish OIL; Calcium; Vitamins

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