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Protonix (Pantoprazole) - Adverse Event Reports - All Cases - Pruritus

 



Index of reports > All cases (68) > Cases with Pruritus (7)

Below is the selection of adverse event reports related to Protonix (Pantoprazole) that includes all cases where reactions include pruritus.

Adverse event in 52 year old female receiving Protonix (Pantoprazole)

Reported by a pharmacist from United States on 2007-06-19

Patient: 52 year old female, weighing 84.0 kg (184.8 pounds)

Adverse reactions / side effects: Pruritus, Angioedema

Adverse event resulted in: hospitalization

Suspect drug(s):
Protonix (Pantoprazole)



Adverse event in 69 year old female receiving Protonix (Pantoprazole)

Reported by a individual with unspecified qualification from United States on 2007-05-04

Patient: 69 year old female

Adverse reactions / side effects: Back Pain, Rash Generalised, Pruritus, Swelling Face, Drug Ineffective, Head Injury, Hypotension, Chills, Erythema, Syncope, Fatigue, Dehydration, Eye Swelling, Back Injury, Cough

Adverse event resulted in: hospitalization

Suspect drug(s):
Nitrofurantoin Monohydrate / Macrocrystals
    Dosage: see image
    Administration route: Oral
    Indication: Cystitis
    Start date: 2006-11-16
    End date: 2006-11-22

Nitrofurantoin Monohydrate / Macrocrystals
    Dosage: see image
    Administration route: Oral
    Indication: Cystitis
    Start date: 2006-11-30
    End date: 2006-12-05

Nitrofurantoin Monohydrate / Macrocrystals
    Dosage: see image
    Administration route: Oral
    Indication: Cystitis
    Start date: 2007-02-06
    End date: 2007-02-11

Protonix
    Dosage: oral
    Administration route: Oral
    Start date: 2006-12-10
    End date: 2007-01-18

Protonix
    Dosage: oral
    Administration route: Oral
    End date: 2007-04-03

Other drugs received by patient: Levothyroxine Sodium; Alendronate Sodium; Triamterene and Hydrochlorothiazide



Adverse event in male receiving Protonix (Pantoprazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-05

Patient: male

Adverse reactions / side effects: Flushing, Dyspnoea, Hypersensitivity, Pruritus, Syncope, Skin Burning Sensation, Rash, Throat Tightness

Adverse event resulted in: life threatening event

Suspect drug(s):
Protonix
    Dosage: unknown
    Administration route: Oral
    Indication: Dyspepsia
    Start date: 2006-01-01
    End date: 2006-01-01

Protonix
    Dosage: 40 mg
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2006-08-01
    End date: 2006-08-01

Other drugs received by patient: Proscar; Zocor; Ritalin; Lasix; Cipro; Flonase; Mobic; Benicar; Singulair; Celexa; Lactulose



Adverse event in female receiving Protonix (Pantoprazole)

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 89 year old female receiving Protonix (Pantoprazole)

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

Patient: 89 year old female, weighing 49.9 kg (109.8 pounds)

Adverse reactions / side effects: Blood Pressure Systolic Decreased, Burning Sensation, Pruritus

Adverse event resulted in: hospitalization

Suspect drug(s):
Protonix (Pantoprazole)



Adverse event in female receiving Protonix (Pantoprazole)

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 Protonix (Pantoprazole)

Reported by a pharmacist from United States on 2007-01-25

Patient: female, weighing 68.0 kg (149.7 pounds)

Adverse reactions / side effects: Pruritus, Rash Generalised, Urticaria

Adverse event resulted in: hospitalization

Suspect drug(s):
Protonix (Pantoprazole)

Other drugs received by patient: Albuterol; Birth Control Pills

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