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Sandostatin (Octreotide) - Fatigue - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Fatigue (68)

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

 Reports 1 - 30 of 68   Next >>

Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-08-27

Patient: female

Reactions: Pneumonia, Blood Pressure Systolic Increased, Fall, Suicidal Ideation, Tremor, Abdominal Discomfort, Fatigue, Malaise, Diarrhoea, Feeling Jittery, Psychiatric Symptom, Mental Disorder, Vasculitis, Depressed Mood

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: unk ukn, unk
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-11

Sandostatin LAR
    Dosage: 20 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-26



Possible Sandostatin side effects in female

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-08-27

Patient: female

Reactions: Abdominal Pain, Fatigue, Diarrhoea, Arthralgia, Pain in Extremity, Insomnia

Drug(s) suspected as cause:
Sandostatin
    Dosage: 50 ug, bid
    Indication: Acromegaly
    Start date: 2009-07-07

Sandostatin LAR
    Dosage: 20 mg, monthly
    Indication: Acromegaly
    Start date: 2009-07-24

Sandostatin LAR
    Dosage: 20 mg, every 4 weeks

Sandostatin LAR
    Dosage: 30 mg, monthly



Possible Sandostatin side effects in male

Reported by a consumer/non-health professional from Canada on 2012-08-27

Patient: male

Reactions: Abdominal Pain, Productive Cough, Pruritus, Nasopharyngitis, Metastases To Liver, Pyrexia, Faecal Volume Increased, Hot Flush, Fatigue, Cough, Decreased Appetite, Abdominal Pain Lower, Vomiting, Pain in Extremity, Nausea, Abnormal Faeces, Injection Site Pain, Skin Plaque, Flushing, Abdominal Mass, Arthralgia, Gastrointestinal Neoplasm, Diarrhoea, Dysphonia, Neoplasm Malignant, Visual Impairment, Vision Blurred, Lacrimation Increased, Depressed Mood

Drug(s) suspected as cause:
Sandostatin
    Dosage: 100 ug, tid
    Start date: 2010-03-01

Sandostatin
    Indication: Neuroendocrine Tumour
    End date: 2008-01-01

Sandostatin LAR
    Dosage: 30 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2010-03-13

Sandostatin LAR
    Dosage: 40 mg, every 4 weeks

Sandostatin LAR
    Dosage: 30 mg every 4 weeks

Other drugs received by patient: Antibiotics; Morphine



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-08-27

Patient: female

Reactions: Flushing, Fatigue, Diarrhoea, Pain in Extremity, Pain, Dizziness, Muscle Spasms

Drug(s) suspected as cause:
Sandostatin
    Dosage: unk ukn, unk
    Indication: Neuroendocrine Tumour

Sandostatin
    Dosage: every 12 hrs
    Start date: 2012-08-14

Sandostatin LAR
    Dosage: 30 mg, every 3 weeks
    Start date: 2012-07-04

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Indication: Neuroendocrine Tumour
    Start date: 2012-07-04



Possible Sandostatin side effects in male

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

Patient: male

Reactions: Jaundice, Abdominal Pain, Blood Bilirubin Increased, Confusional State, Agitation, Weight Decreased, Bile Duct Obstruction, Urinary Incontinence, Constipation, Loss of Consciousness, Malaise, Fatigue, Pleural Effusion, Cardiac Failure Congestive, Cough, Decreased Appetite, Lethargy, Blood Pressure Increased, Dyspnoea, Restlessness, Pain in Extremity, Ascites, Discomfort, Heart Rate Decreased, Abdominal Mass, Syncope, Micturition Disorder, Joint Swelling, Urine Colour Abnormal, Dehydration, Asthenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin

Sandostatin LAR
    Dosage: 30 mg, every 3 weeks

Sandostatin LAR
    Dosage: 20 mg, once in a month
    Indication: Neuroendocrine Tumour
    Start date: 2011-02-28

Other drugs received by patient: Sutent



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-08-13

Patient: female

Reactions: Death, Fatigue, Decreased Appetite

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Sandostatin
    Indication: Crohn's Disease

Sandostatin
    Dosage: 500 ug, bid
    Indication: Neoplasm Malignant
    Start date: 2012-06-28

Sandostatin LAR
    Dosage: 20 mg once a month
    Indication: Neoplasm Malignant
    Start date: 2012-06-28
    End date: 2012-06-28

Sandostatin LAR
    Indication: Crohn's Disease



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-08-07

Patient: female

Reactions: Fatigue, Decreased Appetite

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: 500 ug, bid
    Indication: Neoplasm Malignant
    Start date: 2012-06-28

Sandostatin
    Indication: Crohn's Disease

Sandostatin LAR
    Indication: Crohn's Disease

Sandostatin LAR
    Dosage: 20 mg once a month
    Indication: Neoplasm Malignant
    Start date: 2012-06-28
    End date: 2012-06-28



Possible Sandostatin side effects in male

Reported by a consumer/non-health professional from Canada on 2012-08-06

Patient: male

Reactions: Blood Bilirubin Increased, Confusional State, Weight Decreased, Abdominal Pain, Agitation, Jaundice, Bile Duct Obstruction, Urinary Incontinence, Constipation, Loss of Consciousness, Fatigue, Malaise, Pleural Effusion, Cough, Decreased Appetite, Lethargy, Cardiac Failure Congestive, Blood Pressure Increased, Dyspnoea, Pain in Extremity, Restlessness, Discomfort, Ascites, Syncope, Abdominal Mass, Heart Rate Decreased, Joint Swelling, Micturition Disorder, Urine Colour Abnormal, Dehydration, Asthenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin

Sandostatin LAR
    Dosage: 20 mg, once in a month
    Indication: Neuroendocrine Tumour
    Start date: 2011-02-28

Sandostatin LAR
    Dosage: 30 mg, every 3 weeks

Other drugs received by patient: Sutent



Possible Sandostatin side effects in male

Reported by a physician from Canada on 2012-08-03

Patient: male

Reactions: Abdominal Pain, Nasopharyngitis, Pruritus, Metastases To Liver, Faecal Volume Increased, Fatigue, Hot Flush, Decreased Appetite, Abdominal Pain Lower, Vomiting, Nausea, Pain in Extremity, Abnormal Faeces, Injection Site Pain, Skin Plaque, Flushing, Abdominal Mass, Diarrhoea, Gastrointestinal Neoplasm, Neoplasm Malignant, Dysphonia, Arthralgia, Visual Impairment, Vision Blurred, Lacrimation Increased, Depressed Mood

Drug(s) suspected as cause:
Sandostatin
    Dosage: 100 ug, tid
    Start date: 2010-03-01

Sandostatin
    Indication: Neuroendocrine Tumour
    End date: 2008-01-01

Sandostatin LAR
    Dosage: 40 mg, every 4 weeks

Sandostatin LAR
    Dosage: 30 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2010-03-13

Sandostatin LAR
    Dosage: 30 mg every 4 weeks

Other drugs received by patient: Morphine Sulfate



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-08-01

Patient: female

Reactions: Haemorrhage, Rectal Haemorrhage, Malaise, Fatigue, White Blood Cell Count Increased, Lethargy, Vomiting, Loss of Control of Legs, Nausea, Urinary Tract Infection, Injection Site Pain, Facial Pain, Blood Creatine Increased, Tremor, Discomfort, Haemoglobin Decreased, Diarrhoea, Liver Abscess, Blood Pressure Decreased

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Indication: Carcinoid Tumour

Sandostatin LAR
    Dosage: 20 mg, every 4 weeks
    Start date: 2011-07-05

Sandostatin LAR
    Dosage: 20 mg, qmo
    Indication: Carcinoid Tumour
    Start date: 2011-07-05

Other drugs received by patient: Norfloxacin



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-07-25

Patient: female, weighing 56.7 kg (124.7 pounds)

Reactions: Confusional State, Weight Decreased, Incorrect Route of Drug Administration, Drug Ineffective, Blood Thyroid Stimulating Hormone Increased, Incorrect Storage of Drug, Weight Increased, Injection Site Discomfort, Injection Site Erythema, Malaise, Fatigue, Hot Flush, Oedema Peripheral, Dizziness, Abdominal Distension, Mood Swings, Muscle Spasms, Injection Site Mass, Pain in Extremity, Blood Pressure Systolic Increased, Injection Site Pain, Thyroxine Increased, Flushing, Diarrhoea, Visual Impairment, Vertigo, Feeling Abnormal

Drug(s) suspected as cause:
Sandostatin
    Dosage: 0.75 ml, bid

Sandostatin
    Dosage: 7 ug, qd
    Indication: Carcinoid Syndrome
    Start date: 2008-11-06

Sandostatin
    Dosage: 150 ug, tid (prn)
    Start date: 2011-09-20

Sandostatin
    Dosage: 0.75 ml, tid prn

Sandostatin LAR
    Dosage: 30 mg, qmo

Sandostatin LAR
    Dosage: 30 mg, every four weeks
    Indication: Carcinoid Syndrome
    Start date: 2007-03-20

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Start date: 2007-03-20

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Start date: 2012-05-04



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-07-24

Patient: female

Reactions: Abdominal Pain, Blood Growth Hormone Increased, Blood Pressure Systolic Increased, Mass, Necrosis, Acne, Loss of Consciousness, Abdominal Pain Upper, Fatigue, Arthralgia, Injection Site Calcification, Dizziness, Asthenia

Drug(s) suspected as cause:
Sandostatin
    Dosage: 3 df, (3 times per night)
    Indication: Headache

Sandostatin LAR
    Dosage: 40 mg every 3 weeks
    Indication: Acromegaly
    Start date: 2004-07-15

Other drugs received by patient: Avalide; Avapro



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-07-19

Patient: female

Reactions: Fatigue, Decreased Appetite

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Indication: Crohn's Disease

Sandostatin
    Dosage: 500 ug, bid
    Indication: Neoplasm Malignant
    Start date: 2012-06-28

Sandostatin LAR
    Indication: Crohn's Disease

Sandostatin LAR
    Dosage: 20 mg, qmo
    Indication: Neoplasm Malignant
    Start date: 2012-06-28



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-07-17

Patient: female

Reactions: Abdominal Pain, Flatulence, Pain, Constipation, Fall, Abdominal Pain Upper, Herpes Zoster, Fatigue, Malaise, Dizziness, Abdominal Distension, Anuria, Blood Pressure Increased, Back Pain, Humerus Fracture, Gastrointestinal Motility Disorder, Vomiting, Pain in Extremity, Nausea, Flushing, Arthralgia, Diarrhoea, Ocular Hyperaemia, Flank Pain, Vision Blurred, Asthenia, Neuralgia, Abdominal Adhesions

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: 100 ug, tid
    Indication: Small Intestine Carcinoma

Sandostatin LAR
    Dosage: 30 mg, qmo

Sandostatin LAR
    Dosage: 30 mg, qmo

Sandostatin LAR
    Dosage: 30 mg, tiw
    Indication: Small Intestine Carcinoma
    Start date: 2009-05-26

Sandostatin LAR
    Dosage: 30 mg, tiw

Sandostatin LAR
    Dosage: 30 mg, tiw

Other drugs received by patient: Xeloda; Capecitabine



Possible Sandostatin side effects in female

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-07-04

Patient: female

Reactions: Pneumonia, Blood Pressure Systolic Increased, Fall, Suicidal Ideation, Abdominal Discomfort, Fatigue, Malaise, Diarrhoea, Psychiatric Symptom, Mental Disorder, Vasculitis, Depressed Mood

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: unk ukn, unk
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-11

Sandostatin LAR
    Dosage: 20 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-26



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-06-28

Patient: female

Reactions: Abdominal Pain, Blood Pressure Increased, Blood Growth Hormone Increased, Mass, Blood Pressure Systolic Increased, Necrosis, Acne, Loss of Consciousness, Abdominal Pain Upper, Fatigue, Injection Site Calcification, Arthralgia, Dizziness, Asthenia

Drug(s) suspected as cause:
Sandostatin
    Dosage: 3 df, (3 times per night)
    Indication: Headache

Sandostatin LAR
    Dosage: 40 mg every 3 weeks
    Indication: Acromegaly
    Start date: 2004-07-15

Other drugs received by patient: Avalide



Possible Sandostatin side effects in female

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-06-26

Patient: female

Reactions: Blood Pressure Systolic Increased, Fall, Suicidal Ideation, Abdominal Discomfort, Fatigue, Malaise, Diarrhoea, Psychiatric Symptom, Mental Disorder, Vasculitis, Depressed Mood

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: unk ukn, unk
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-11

Sandostatin LAR
    Dosage: 20 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-26



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-06-06

Patient: female, weighing 56.7 kg (124.7 pounds)

Reactions: Incorrect Route of Drug Administration, Confusional State, Weight Decreased, Drug Ineffective, Blood Thyroid Stimulating Hormone Increased, Incorrect Storage of Drug, Weight Increased, Injection Site Erythema, Fatigue, Injection Site Discomfort, Malaise, Hot Flush, Oedema Peripheral, Dizziness, Abdominal Distension, Mood Swings, Muscle Spasms, Injection Site Mass, Blood Pressure Systolic Increased, Pain in Extremity, Injection Site Pain, Thyroxine Increased, Flushing, Diarrhoea, Visual Impairment, Vertigo, Feeling Abnormal

Drug(s) suspected as cause:
Sandostatin
    Dosage: 150 ug, tid (prn)
    Start date: 2011-09-20

Sandostatin
    Dosage: 0.75 ml, bid

Sandostatin
    Dosage: 0.75 ml, tid prn

Sandostatin
    Dosage: 7 ug, qd
    Indication: Carcinoid Syndrome
    Start date: 2008-11-06

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Start date: 2012-05-04

Sandostatin LAR
    Dosage: 30 mg, every four weeks
    Indication: Carcinoid Syndrome
    Start date: 2007-03-20

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Start date: 2007-03-20

Sandostatin LAR
    Dosage: 30 mg, qmo



Possible Sandostatin side effects in male

Reported by a physician from Canada on 2012-06-01

Patient: male

Reactions: Abdominal Pain, Pruritus, Metastases To Liver, Faecal Volume Increased, Fatigue, Hot Flush, Decreased Appetite, Abdominal Pain Lower, Vomiting, Nausea, Pain in Extremity, Abnormal Faeces, Injection Site Pain, Skin Plaque, Flushing, Abdominal Mass, Arthralgia, Neoplasm Malignant, Dysphonia, Gastrointestinal Neoplasm, Diarrhoea, Visual Impairment, Vision Blurred, Lacrimation Increased, Depressed Mood

Drug(s) suspected as cause:
Sandostatin
    Dosage: 100 ug, tid
    Start date: 2010-03-01

Sandostatin
    Indication: Neuroendocrine Tumour
    End date: 2008-01-01

Sandostatin LAR
    Dosage: 30 mg every 4 weeks

Sandostatin LAR
    Dosage: 40 mg, every 4 weeks

Sandostatin LAR
    Dosage: 30 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2010-03-13

Other drugs received by patient: Morphine



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-05-30

Patient: female

Reactions: Nasopharyngitis, Flatulence, Neoplasm Progression, Synovial Cyst, Fatigue, Malaise, Oedema Peripheral, Proctalgia, Cough, Viral Infection, Nausea, Abnormal Faeces, Faecal Incontinence, Diarrhoea, Joint Swelling, Influenza Like Illness

Drug(s) suspected as cause:
Sandostatin
    Indication: Neuroendocrine Carcinoma
    Start date: 2011-11-22

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Indication: Neuroendocrine Carcinoma
    Start date: 2011-11-25

Other drugs received by patient: Other Anti-Asthmatics, Inhalants



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-05-28

Patient: female, weighing 56.7 kg (124.7 pounds)

Reactions: Incorrect Route of Drug Administration, Confusional State, Weight Decreased, Blood Thyroid Stimulating Hormone Increased, Incorrect Storage of Drug, Weight Increased, Fatigue, Injection Site Discomfort, Injection Site Erythema, Malaise, Hot Flush, Oedema Peripheral, Abdominal Distension, Dizziness, Mood Swings, Muscle Spasms, Injection Site Mass, Pain in Extremity, Blood Pressure Systolic Increased, Injection Site Pain, Thyroxine Increased, Flushing, Diarrhoea, Visual Impairment, Vertigo, Feeling Abnormal

Drug(s) suspected as cause:
Sandostatin
    Dosage: 150 ug, tid (prn)
    Start date: 2011-09-20

Sandostatin
    Dosage: 7 ug, qd
    Indication: Carcinoid Syndrome
    Start date: 2008-11-06

Sandostatin
    Dosage: 0.75 ml, tid prn

Sandostatin
    Dosage: 0.75 ml, bid

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks

Sandostatin LAR
    Dosage: 30 mg, every four weeks
    Indication: Carcinoid Syndrome
    Start date: 2007-03-20

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Start date: 2007-03-20

Sandostatin LAR
    Dosage: 30 mg, qmo



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-05-28

Patient: female

Reactions: Blood Pressure Systolic Increased, Fall, Suicidal Ideation, Abdominal Discomfort, Malaise, Fatigue, Diarrhoea, Psychiatric Symptom, Mental Disorder, Vasculitis, Depressed Mood

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: unk ukn, unk
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-11

Sandostatin LAR
    Dosage: 20 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-26



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-05-25

Patient: female

Reactions: Blood Pressure Systolic Increased, Fall, Suicidal Ideation, Abdominal Discomfort, Fatigue, Malaise, Diarrhoea, Psychiatric Symptom, Mental Disorder, Vasculitis, Depressed Mood

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: unk ukn, unk
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-11

Sandostatin LAR
    Dosage: 20 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-26



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-05-22

Patient: female

Reactions: Nasopharyngitis, Flatulence, Neoplasm Progression, Synovial Cyst, Malaise, Fatigue, Oedema Peripheral, Cough, Proctalgia, Viral Infection, Nausea, Abnormal Faeces, Faecal Incontinence, Diarrhoea, Joint Swelling, Influenza Like Illness

Drug(s) suspected as cause:
Sandostatin
    Indication: Neuroendocrine Carcinoma
    Start date: 2011-11-22

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Indication: Neuroendocrine Carcinoma
    Start date: 2011-11-25

Other drugs received by patient: Other Anti-Asthmatics, Inhalants



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-05-18

Patient: female

Reactions: Abdominal Pain, Blood Growth Hormone Increased, Blood Pressure Systolic Increased, Mass, Necrosis, Acne, Abdominal Pain Upper, Fatigue, Injection Site Calcification, Arthralgia, Asthenia

Drug(s) suspected as cause:
Sandostatin
    Dosage: 3 df, (3 times per night)
    Indication: Headache

Sandostatin LAR
    Dosage: 40 mg every 3 weeks
    Indication: Acromegaly
    Start date: 2004-07-15



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-05-14

Patient: female

Reactions: Abdominal Pain, Flatulence, Pain, Constipation, Fall, Abdominal Pain Upper, Herpes Zoster, Fatigue, Malaise, Abdominal Distension, Dizziness, Back Pain, Blood Pressure Increased, Humerus Fracture, Vomiting, Nausea, Pain in Extremity, Flushing, Diarrhoea, Arthralgia, Ocular Hyperaemia, Flank Pain, Vision Blurred, Asthenia, Neuralgia, Abdominal Adhesions

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: 100 ug, tid
    Indication: Small Intestine Carcinoma

Sandostatin LAR
    Dosage: 30 mg, qmo

Sandostatin LAR
    Dosage: 30 mg, every 3 weeks

Sandostatin LAR
    Dosage: 30 mg, qmo

Sandostatin LAR
    Dosage: 30 mg, tiw
    Indication: Small Intestine Carcinoma
    Start date: 2009-05-26

Sandostatin LAR
    Dosage: 30 mg, every three weeks

Other drugs received by patient: Xeloda; Capecitabine



Possible Sandostatin side effects in female

Reported by a consumer/non-health professional from Canada on 2012-05-09

Patient: female, weighing 56.7 kg (124.7 pounds)

Reactions: Incorrect Route of Drug Administration, Weight Decreased, Confusional State, Blood Thyroid Stimulating Hormone Increased, Incorrect Storage of Drug, Weight Increased, Hot Flush, Malaise, Injection Site Erythema, Fatigue, Oedema Peripheral, Abdominal Distension, Dizziness, Mood Swings, Muscle Spasms, Injection Site Mass, Pain in Extremity, Blood Pressure Systolic Increased, Injection Site Pain, Thyroxine Increased, Flushing, Diarrhoea, Visual Impairment, Vertigo, Feeling Abnormal

Drug(s) suspected as cause:
Sandostatin
    Dosage: 150 ug, tid (prn)
    Start date: 2011-09-20

Sandostatin
    Dosage: 0.75 ml, bid

Sandostatin
    Dosage: 0.75 ml, tid prn

Sandostatin
    Dosage: 7 ug, qd
    Indication: Carcinoid Syndrome
    Start date: 2008-11-06

Sandostatin LAR
    Dosage: 30 mg, qmo
    Indication: Carcinoid Syndrome
    Start date: 2007-03-20

Sandostatin LAR
    Dosage: 30 mg, qmo

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Start date: 2007-03-20

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks



Possible Sandostatin side effects in male

Reported by a physician from Canada on 2012-05-09

Patient: male

Reactions: Weight Decreased, Abdominal Pain, Nasopharyngitis, Mouth Ulceration, Skin Burning Sensation, Oropharyngeal Pain, Erythema, Gastritis, Haematemesis, Abdominal Discomfort, Hot Flush, Fatigue, Injection Site Induration, Decreased Appetite, Cough, Injection Site Mass, Vomiting, Stomatitis, Nausea, Injection Site Pain, Diarrhoea, Hypophagia, Rash Maculo-Papular, Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: 500 ug, bid
    Start date: 2011-08-25

Sandostatin
    Dosage: 150 ug, bid
    Start date: 2011-02-14
    End date: 2011-02-17

Sandostatin
    Dosage: 250 ug, bid
    Start date: 2011-06-08

Sandostatin
    Dosage: 500 ug, bid
    Start date: 2011-08-25

Sandostatin
    Dosage: 100 ug, tid
    Indication: Neuroendocrine Tumour
    Start date: 2011-02-01
    End date: 2011-02-14

Sandostatin
    Dosage: 500 ug, tid

Sandostatin LAR
    Dosage: 40 mg, every three weeks
    End date: 2011-06-08

Sandostatin LAR
    Dosage: 30 mg, tiw

Sandostatin LAR
    Dosage: 40 mg every three weeks
    End date: 2011-05-21

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Indication: Neuroendocrine Tumour
    Start date: 2009-09-10

Sandostatin LAR
    Dosage: 40 mg, every 4 weeks

Sandostatin LAR
    Dosage: 40 mg, qmo

Other drugs received by patient: Mesalamine; Insulin; Aspirin; Gravol TAB; Fragmin; Pantoprazole Sodium



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-05-09

Patient: female

Reactions: Viral Infection, Nasopharyngitis, Nausea, Abnormal Faeces, Flatulence, Faecal Incontinence, Synovial Cyst, Fatigue, Malaise, Diarrhoea, Joint Swelling, Oedema Peripheral, Proctalgia, Cough, Influenza Like Illness

Drug(s) suspected as cause:
Sandostatin
    Indication: Neuroendocrine Carcinoma
    Start date: 2011-11-22

Sandostatin LAR
    Dosage: 30 mg, every 4 weeks
    Indication: Neuroendocrine Carcinoma
    Start date: 2011-11-25

Other drugs received by patient: Other Anti-Asthmatics, Inhalants



Possible Sandostatin side effects in female

Reported by a physician from Canada on 2012-04-30

Patient: female

Reactions: Abdominal Discomfort, Malaise, Fatigue, Blood Pressure Systolic Increased, Diarrhoea, Mental Disorder, Vasculitis, Fall

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Sandostatin
    Dosage: unk ukn, unk
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-11

Sandostatin LAR
    Dosage: 20 mg, qmo
    Indication: Neuroendocrine Tumour
    Start date: 2011-07-26



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