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Carafate (Sucralfate) - Nausea - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Nausea (5)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Carafate (Sucralfate) where reactions include nausea. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Carafate side effects in 50 year old female

Reported by a consumer/non-health professional from United States on 2012-08-16

Patient: 50 year old female

Reactions: Vomiting, Eye Irritation, Nausea, Therapeutic Response Unexpected, Foreign Body, Treatment Noncompliance, Abdominal Pain Upper, Off Label Use, Incorrect Drug Administration Duration, Overdose, Conjunctivitis Infective, Gallbladder Disorder, Gastrooesophageal Reflux Disease, Feeling Abnormal, Eye Pruritus

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Carafate
    Dosage: unk, unk

Drug Therapy NOS
    Indication: Conjunctivitis Infective

Prevacid 24 HR
    Dosage: 15 mg, qd
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease

Prevacid 24 HR
    Dosage: 30 mg, qd
    Administration route: Oral



Possible Carafate side effects in 50 year old female

Reported by a consumer/non-health professional from United States on 2012-08-15

Patient: 50 year old female

Reactions: Vomiting, Nausea, Eye Irritation, Foreign Body, Treatment Noncompliance, Abdominal Pain Upper, Off Label Use, Overdose, Incorrect Drug Administration Duration, Conjunctivitis Infective, Gallbladder Disorder, Gastrooesophageal Reflux Disease, Feeling Abnormal, Eye Pruritus

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Carafate
    Dosage: unk, unk

Drug Therapy NOS
    Indication: Conjunctivitis Infective

Prevacid 24 HR
    Dosage: 30 mg, qd
    Administration route: Oral

Prevacid 24 HR
    Dosage: 15 mg, qd
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease



Possible Carafate side effects in 60 year old female

Reported by a consumer/non-health professional from United States on 2012-06-29

Patient: 60 year old female, weighing 108.9 kg (239.5 pounds)

Reactions: Vomiting, Haemorrhage, Nausea, Condition Aggravated, Headache, Eczema, Epistaxis

Drug(s) suspected as cause:
Amicar
    Indication: Product Used FOR Unknown Indication

Carafate
    Indication: Product Used FOR Unknown Indication

Desonide
    Indication: Product Used FOR Unknown Indication

Diflorasone Diacetate
    Indication: Product Used FOR Unknown Indication

Fluticasone Propionate
    Indication: Product Used FOR Unknown Indication
    End date: 2012-04-01

Lidocaine
    Indication: Product Used FOR Unknown Indication

Lysteda
    Indication: Platelet Disorder

Metronidazole
    Administration route: Topical
    Indication: Product Used FOR Unknown Indication

Polymyxin B Sulfate
    Indication: Product Used FOR Unknown Indication

Tretinoin
    Indication: Product Used FOR Unknown Indication

Vitamin E
    Indication: Product Used FOR Unknown Indication

Other drugs received by patient: Acetaminophen



Possible Carafate side effects in male

Reported by a individual with unspecified qualification from United States on 2012-06-13

Patient: male

Reactions: Vomiting, Malaise, Nausea

Drug(s) suspected as cause:
Carafate



Possible Carafate side effects in 77 year old female

Reported by a physician from United States on 2012-03-16

Patient: 77 year old female

Reactions: Vomiting, Nausea, Coagulopathy, Duodenal Ulcer, Haematemesis, Gastritis, Blood Potassium Decreased, Oesophagitis, Melaena

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Abarelix (Abarelix) Unknown
    Indication: Product Used FOR Unknown Indication

Avastin
    Start date: 2006-08-29

Avastin
    Dosage: q 3 weeks, intravenous
    Indication: Breast Cancer Metastatic
    Start date: 2006-08-29

Avastin
    Dosage: q 3 weeks, intravenous
    Indication: Breast Cancer Metastatic
    Start date: 2007-01-08

Carafate
    Indication: Product Used FOR Unknown Indication
    Start date: 2007-01-01

Paclitaxel
    Dosage: 416 mg,
    Indication: Breast Cancer
    Start date: 2006-08-29

Paclitaxel
    Dosage: 416 mg,
    Indication: Breast Cancer
    Start date: 2007-01-08

Other drugs received by patient: Zocor (Simvastatin) Unknown UNK TO UNK; Miacalcin (Calcitonin, Salmon) UNK TO UNK; Maalox / 00082501 / (Aluminium Hydroxide, Magnesium Hydroxide) UNK TO UN; OS-CAL / 00108001 / (Calcium Carbonate) Unknown UNK TO UNK; Zometa (Zoledronic Acid) UNK TO UNK; Magnesium (Magnesium) Unknown UNK TO UNK; Glycerin / 00200601 / (Glycerol) Unknown UNK TO UNK; Monistat (Miconazole Nitrate) Unknown UNK TO UNK; Triple-MIX Mouth Wash Unknown UNK TO UNK; Esomeprazole Magnesium (Esomeprazole Magnesium) Unknown UNK TO UNK; Diphenhydramine Hydrochloride (Diphenhydramine Hydrochloride) Unknown; Senokot / 00142201 / (Senna Alexandrina) Unknown UNK TO UNK; Aloxi (Palonosetron Hydrochloride) UNK TO UNK; Dexamethasone (Dexamethasone) Unknown UNK TO UNK; Astelin / 00884002 / (Azelastine Hydrochloride) UNK TO UNK; Compazine / 00013302 / (Prochlorperazine Edisylate) UNK TO UNK; Percocet / 00867901 / (Oxycodone Hydrochloride, Paracetamol) UNK TO UNK; Phenergan / 00033001 / (Promethazine) UNK TO UNK

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