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Prevacid (Lansoprazole) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (17)

     Nausea (4)Skin Exfoliation (4)Urticaria (4)Staphylococcal Sepsis (4)Respiratory Syncytial Virus Infection (4)Blood Pressure Inadequately Controlled (4)Dizziness (4)Neutropenia (4)Auricular Swelling (3)Sepsis (3)

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

Adverse event in female receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-10-30

Patient: female, weighing 22.7 kg (49.9 pounds)

Adverse reactions / side effects: Bacteraemia, Drug Hypersensitivity, Sepsis, Skin Lesion, Neutropenia, Staphylococcal Sepsis, Respiratory Syncytial Virus Infection

Adverse event resulted in: hospitalization

Suspect drug(s):
Amlodipine
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-05-01
    End date: 2007-10-02

Enalapril Maleate
    Dosage: text:1 tablet-freq:frequency: daily
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-05-01
    End date: 2006-06-01

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

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

Other drugs received by patient: Prednisolone; Cyclosporine



Adverse event in 58 year old female receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from United States on 2007-10-30

Patient: 58 year old female, weighing 56.7 kg (124.7 pounds)

Adverse reactions / side effects: HIP Fracture, Osteopenia, Fall

Adverse event resulted in: hospitalization

Suspect drug(s):
Prevacid (Lansoprazole)

Other drugs received by patient: Boniva (Ibandronate Sodium); Calcium Supplement (Calcium); Acetaminophen



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

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

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

Other drugs received by patient: Prednisolone; Cyclosporine; Cozaar



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

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

Patient: 2 year old female, weighing 22.7 kg (49.9 pounds)

Adverse reactions / side effects: LIP Swelling, Skin Chapped, Swelling Face, Skin Exfoliation, Urticaria, Helicobacter Infection, Skin Induration, Staphylococcal Sepsis, Respiratory Syncytial Virus Infection, Bone Marrow Disorder, Auricular Swelling, Skin Haemorrhage, Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Amlodipine
    Dosage: per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-04-01
    End date: 2007-10-02

Enalapril Maleate
    Dosage: 1 tab., 1 in 1 d, per oral; 1 tab., 1 in 1 d, per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-04-01
    End date: 2006-06-01

Enalapril Maleate
    Dosage: 1 tab., 1 in 1 d, per oral; 1 tab., 1 in 1 d, per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-09-07
    End date: 2007-10-02

Prevacid
    Indication: Drug USE FOR Unknown Indication
    Start date: 2004-01-01
    End date: 2006-06-01

Other drugs received by patient: Prednisone; Cyclosporine (Ciclosporin)



Adverse event in 93 year old female receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from United States on 2007-10-17

Patient: 93 year old female

Adverse reactions / side effects: HIP Fracture

Adverse event resulted in: hospitalization

Suspect drug(s):
Prevacid (Lansoprazole)



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

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

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

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

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



Adverse event in 40 year old male receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-07-03

Patient: 40 year old male

Adverse reactions / side effects: Drug Interaction, Anticonvulsant Drug Level Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Phenytoin Sodium
    Indication: Convulsion

Prevacid
    End date: 2007-05-22

Protonix
    Dosage: 40 mg, 1 in 1 d, oral
    Administration route: Oral
    Start date: 2007-05-23

Other drugs received by patient: Multivitamin; Gabapentin



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):
Acetylsalicylic Acid SRT
    Indication: Cardiovascular Event Prophylaxis

Amoxicillin
    Indication: Pneumonia

Chantix
    Indication: EX-Smoker

Drug, Unspecified

Prednisone TAB
    Indication: Crohn's Disease

Prevacid
    Indication: Gastrooesophageal Reflux Disease

Prilosec
    Indication: Gastrooesophageal Reflux Disease

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

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



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):
Acetylsalicylic Acid SRT
    Indication: Cardiovascular Event Prophylaxis

Amoxicillin
    Indication: Pneumonia

Chantix
    Indication: EX-Smoker

Drug, Unspecified

Prednisone TAB
    Indication: Crohn's Disease

Prevacid
    Indication: Gastrooesophageal Reflux Disease

Prilosec
    Indication: Gastrooesophageal Reflux Disease

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

Other drugs received by patient: Drug, Unspecified; Asacol



Adverse event in 57 year old male receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from United States on 2007-04-27

Patient: 57 year old male, weighing 124.7 kg (274.3 pounds)

Adverse reactions / side effects: Neuropathy, Rash Generalised, Skin Exfoliation, Diabetes Mellitus, Condition Aggravated, Fall, Loss of Consciousness, Renal Failure, Skin Laceration, Oedema Peripheral, Dehydration, Dizziness, Tenderness, Influenza Like Illness

Adverse event resulted in: hospitalization

Suspect drug(s):
Prevacid (Lansoprazole)

Other drugs received by patient: Prinivil; Topamax; Aspirin; Lipitor; Byetta; Glucophage; Glucotrol; Actos; Plavix; Pepcid



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):
Adalat
    Start date: 2001-02-05

Aspirin
    Start date: 2002-05-06

Benicar
    End date: 2003-08-29

Biaxin

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

Clonidine
    Start date: 1999-03-20

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

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

Heparin
    Start date: 2002-05-06

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

Lopressor
    Start date: 2001-01-01

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

Nitrol
    Start date: 2002-05-06

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

Paxil
    Start date: 1999-03-20

Premarin
    Start date: 2002-02-25

Prevacid
    Start date: 2000-01-10

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

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

Protonix
    Start date: 2001-01-01

Toprol-XL
    Start date: 1999-03-20

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

Vicodin ES



Adverse event in 80 year old male receiving Prevacid (Lansoprazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-06

Patient: 80 year old male

Adverse reactions / side effects: Metabolic Encephalopathy

Adverse event resulted in: hospitalization

Suspect drug(s):
Prevacid (Lansoprazole)

Other drugs received by patient: Baclofen; Lipitor; Metformin HCL; Glipizide; Atenolol; Hydrochlorothiazide; Aspirin; Flomax (Morniflumate)



Adverse event in 82 year old female receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from United States on 2007-02-02

Patient: 82 year old female

Adverse reactions / side effects: Colitis Collagenous

Adverse event resulted in: hospitalization

Suspect drug(s):
Prevacid

Zocor
    Administration route: Oral

Other drugs received by patient: Dilantin; Digoxin; Moxifloxacin Hydrochloride; Coumadin



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):
Adalat
    Start date: 2001-02-05

Aspirin
    Start date: 2002-05-06

Benicar
    End date: 2003-08-29

Biaxin

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

Clonidine
    Start date: 1999-03-20

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

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

Heparin
    Start date: 2002-05-06

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

Lopressor
    Start date: 2001-01-01

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

Nitrol
    Start date: 2002-05-06

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

Paxil
    Start date: 1999-03-20

Premarin
    Start date: 2002-02-25

Prevacid
    Start date: 2000-01-10

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

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

Protonix
    Start date: 2001-01-01

Toprol-XL
    Start date: 1999-03-20

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

Vicodin ES



Adverse event in 80 year old male receiving Prevacid (Lansoprazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-30

Patient: 80 year old male

Adverse reactions / side effects: Dysarthria, General Physical Health Deterioration, Metabolic Encephalopathy

Adverse event resulted in: hospitalization

Suspect drug(s):
Prevacid (Lansoprazole)



Adverse event in 54 year old female receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from Canada on 2007-01-29

Patient: 54 year old female

Adverse reactions / side effects: Confusional State, Drug Dose Omission, Dyspnoea, Wrong Drug Administered, Tachycardia, Drug Interaction, Blood Calcium Increased, Drug Withdrawal Syndrome, Headache, Gastric Haemorrhage, Haemoglobin Decreased, Medication Error, Dizziness

Adverse event resulted in: hospitalization

Suspect drug(s):
Effexor XR
    Dosage: 75 mg 1x per 1 day
    Administration route: Oral
    Indication: Anxiety
    Start date: 2002-01-01

Effexor XR
    Dosage: 75 mg 1x per 1 day
    Administration route: Oral
    Indication: Panic Attack
    Start date: 2002-01-01

Effexor XR
    Dosage: 75 mg 1x per 1 day
    Administration route: Oral
    Indication: Post-Traumatic Stress Disorder
    Start date: 2002-01-01

Pantoloc (Pantoprazole, Tablet, Delayed Release, 0)
    Indication: Gastric Haemorrhage

Prevacid
    Dosage: 30 mg qam
    Administration route: Oral
    Indication: Gastric Haemorrhage
    Start date: 2006-11-13
    End date: 2006-12-12

Other drugs received by patient: Ativan; Naproxen



Adverse event in 77 year old female receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from United States on 2007-01-25

Patient: 77 year old female, weighing 56.6 kg (124.5 pounds)

Adverse reactions / side effects: HIP Fracture

Adverse event resulted in: hospitalization

Suspect drug(s):
Prevacid (Lansoprazole)

Other drugs received by patient: Norvasc; Fosamax

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