Common Pantecta Side Effects


The most commonly reported Pantecta side effects (click to view or check a box to report):

Death (7)
Wheezing (4)
Gastrointestinal Haemorrhage (4)
Fall (3)
Chest Discomfort (3)
Rib Fracture (3)
Osteoporosis (3)
Renal Failure (2)
Hiatus Hernia (2)
Nausea (2)
Ulcer (2)
Hepatic Failure (2)
Urticaria (2)
Bone Densitometry (2)
Anaemia (2)
Colon Cancer (2)
Bronchospasm (2)
Cardiac Failure (2)
Dengue Fever (2)
Haemorrhage (2)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Pantecta Side Effects Reported to FDA



Pantecta Side Effect Report#6130258-2
Bone Densitometry, Fall, Osteoporosis, Rib Fracture
This is a report of a 67-year-old female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Pantecta (dosage: 40 Mg Daily, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Bone Densitometry, Fall, Osteoporosis, Rib Fracture after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Pantecta treatment in female patients, resulting in Bone Densitometry side effect.
Pantecta Side Effect Report#6119908-4
Fall, Hand Fracture, Osteoporosis, Rib Fracture
This report suggests a potential Pantecta Fall side effect(s) that can have serious consequences. A 67-year-old female patient (weight: NA) from Costa Rica was diagnosed with the following symptoms/conditions: NA and used Pantecta (dosage: NA) starting NS. After starting Pantecta the patient began experiencing various side effects, including: Fall, Hand Fracture, Osteoporosis, Rib FractureAdditional drugs used concurrently:
  • Cyanocobalamin
  • Liver Extract
  • Hydralazine Hcl
  • Amino Acids
  • Exforge
  • Insulin
Although Pantecta demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Fall, may still occur.
Pantecta Side Effect Report#6114448-0
Bone Densitometry, Fall, Osteoporosis, Rib Fracture
This Bone Densitometry problem was reported by a physician from Costa Rica. A 67-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Pantecta (dosage: 40 Mg Daily). The following drugs were being taken at the same time: NA. When using Pantecta, the patient experienced the following unwanted symptoms/side effects: Bone Densitometry, Fall, Osteoporosis, Rib FractureAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Bone Densitometry, may become evident only after a product is in use by the general population.
Pantecta Side Effect Report#6047650-7
Abdominal Sepsis, Anastomotic Leak, Bronchopneumonia, Colon Cancer, Gastrointestinal Haemorrhage, Haemorrhage, Ulcer
This Abdominal Sepsis side effect was reported by a physician from Germany. A 58-year-old male patient (weight:NA) experienced the following symptoms/conditions: gastrooesophageal reflux disease,diabetes mellitus,hypertension.The patient was prescribed Pantecta (drug dosage: 40-60 Mg Daily), which was initiated on NS. Concurrently used drugs:
  • Insulin
  • Enalapril
.After starting to take Pantecta the consumer reported adverse symptoms, such as: Abdominal Sepsis, Anastomotic Leak, Bronchopneumonia, Colon Cancer, Gastrointestinal Haemorrhage, Haemorrhage, UlcerThese side effects may potentially be related to Pantecta. The patient was hospitalized.
Pantecta Side Effect Report#6036877-6
Colon Cancer, Gastrointestinal Haemorrhage, Haemorrhage, Ulcer
This is a report of a 58-year-old male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Pantecta (dosage: NA, start time: NS), combined with:
  • Insulin
  • Enalapril Maleate
and developed a serious reaction and side effect(s): Colon Cancer, Gastrointestinal Haemorrhage, Haemorrhage, Ulcer after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Pantecta treatment in male patients, resulting in Colon Cancer side effect. The patient was hospitalized.
Pantecta Side Effect Report#6006925-8
Metastasis
This report suggests a potential Pantecta Metastasis side effect(s) that can have serious consequences. A 63-year-old female patient (weight: NA) from Costa Rica was diagnosed with the following symptoms/conditions: gastroduodenal ulcer,vomiting and used Pantecta (dosage: NA) starting NS. After starting Pantecta the patient began experiencing various side effects, including: MetastasisAdditional drugs used concurrently: NA. Although Pantecta demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Metastasis, may still occur.
Pantecta Side Effect Report#5900110-3
Bronchospasm, Dizziness, Urticaria
This Bronchospasm problem was reported by a health professional from Germany. A 51-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Sep 15, 2008 this consumer started treatment with Pantecta (dosage: NA). The following drugs were being taken at the same time: NA. When using Pantecta, the patient experienced the following unwanted symptoms/side effects: Bronchospasm, Dizziness, UrticariaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Bronchospasm, may become evident only after a product is in use by the general population.
Pantecta Side Effect Report#5888922-6
Gallbladder Cancer, Hypoglycaemia, Rash
This Gallbladder Cancer side effect was reported by a health professional from Costa Rica. A 65-year-old male patient (weight:NA) experienced the following symptoms/conditions: gastritis,upper gastrointestinal haemorrhage,cholangitis,diabetes mellitus.The patient was prescribed Pantecta (drug dosage: NA), which was initiated on
Jan 01, 2004. Concurrently used drugs: NA..After starting to take Pantecta the consumer reported adverse symptoms, such as: Gallbladder Cancer, Hypoglycaemia, RashThese side effects may potentially be related to Pantecta.
Pantecta Side Effect Report#5726737-X
Anaemia
This is a report of a 68-year-old male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: gastrectomy, who was treated with Pantecta (dosage: NA, start time:
Jan 01, 2001), combined with:
  • Novonorm
  • Ferro-grad
  • Lasix
  • Coumadin
  • Eskim
  • Sinvacor
  • Triatec
and developed a serious reaction and side effect(s): Anaemia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Pantecta treatment in male patients, resulting in Anaemia side effect. The patient was hospitalized.
Pantecta Side Effect Report#5663978-4
Osteitis, Pain In Jaw
This report suggests a potential Pantecta Osteitis side effect(s) that can have serious consequences. A 30-year-old male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: NA and used Pantecta (dosage: NA) starting
Jul 01, 2007. After starting Pantecta the patient began experiencing various side effects, including: Osteitis, Pain In JawAdditional drugs used concurrently: NA. Although Pantecta demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Osteitis, may still occur.
Pantecta Side Effect Report#5488313-6
Cyanosis, Pallor, Syncope
This Cyanosis problem was reported by a health professional from Honduras. A 30-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: peptic ulcer. On
Jan 01, 2003 this consumer started treatment with Pantecta (dosage: NA). The following drugs were being taken at the same time: NA. When using Pantecta, the patient experienced the following unwanted symptoms/side effects: Cyanosis, Pallor, SyncopeAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Cyanosis, may become evident only after a product is in use by the general population.
Pantecta Side Effect Report#5476732-3
Dengue Fever, Hepatic Failure, Renal Failure
This Dengue Fever side effect was reported by a physician from Honduras. A 50-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Pantecta (drug dosage: NA), which was initiated on
May 07, 2007. Concurrently used drugs: NA..After starting to take Pantecta the consumer reported adverse symptoms, such as: Dengue Fever, Hepatic Failure, Renal FailureThese side effects may potentially be related to Pantecta. The patient was hospitalized.
Pantecta Side Effect Report#5399423-6
This is a report of a 78-year-old female patient (weight: NA) from Guatemala, suffering from the following health symptoms/conditions: NA, who was treated with Pantecta (dosage: ^df^, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Pantecta treatment in female patients, resulting in Death side effect.
Pantecta Side Effect Report#5386529-0
Dengue Fever, Hepatic Failure, Renal Failure
This report suggests a potential Pantecta Dengue Fever side effect(s) that can have serious consequences. A 50-year-old female patient (weight: NA) from Honduras was diagnosed with the following symptoms/conditions: NA and used Pantecta (dosage: NA) starting
May 07, 2007. After starting Pantecta the patient began experiencing various side effects, including: Dengue Fever, Hepatic Failure, Renal FailureAdditional drugs used concurrently: NA.The patient was hospitalized. Although Pantecta demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dengue Fever, may still occur.
Pantecta Side Effect Report#5220628-9
Neutropenia, White Blood Cell Count Increased
This Neutropenia problem was reported by a consumer or non-health professional from Spain. A 70-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: hepatic cirrhosis. On
Jun 07, 2006 this consumer started treatment with Pantecta (pantoprazole, ) (dosage: Df Oral). The following drugs were being taken at the same time:
  • Ativan
When using Pantecta (pantoprazole, ), the patient experienced the following unwanted symptoms/side effects: Neutropenia, White Blood Cell Count IncreasedAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Neutropenia, may become evident only after a product is in use by the general population.
Pantecta Side Effect Report#5196077-9
Neutropenia
This Neutropenia side effect was reported by a consumer or non-health professional from Spain. A 70-year-old male patient (weight:NA) experienced the following symptoms/conditions: hepatic cirrhosis.The patient was prescribed Pantecta (pantoprazole, ) (drug dosage: Df Oral), which was initiated on
Jun 07, 2006. Concurrently used drugs:
  • Ativan
.After starting to take Pantecta (pantoprazole, ) the consumer reported adverse symptoms, such as: NeutropeniaThese side effects may potentially be related to Pantecta (pantoprazole, ).
Pantecta Side Effect Report#5087246-7
Agranulocytosis
This is a report of a 74-year-old male patient (weight: NA) from Spain, suffering from the following health symptoms/conditions: NA, who was treated with Pantecta (pantoprazole Delayed Release) (dosage: 40 Mg Oral, start time:
Mar 22, 2006), combined with:
  • Nolotil (metamizole Magnesium ) (5 G, Intravenous)
and developed a serious reaction and side effect(s): Agranulocytosis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Pantecta (pantoprazole Delayed Release) treatment in male patients, resulting in Agranulocytosis side effect.
Pantecta Side Effect Report#4879738-8
Dyspnoea, Laryngeal Oedema, Urticaria
This report suggests a potential Pantecta (pantoprazole, Tablet, Delayed Release) Dyspnoea side effect(s) that can have serious consequences. A 42-year-old female patient (weight: NA) from Italy was diagnosed with the following symptoms/conditions: duodenitis,gastritis and used Pantecta (pantoprazole, Tablet, Delayed Release) (dosage: 40 Mg, Oral) starting
Nov 30, 2005. After starting Pantecta (pantoprazole, Tablet, Delayed Release) the patient began experiencing various side effects, including: Dyspnoea, Laryngeal Oedema, UrticariaAdditional drugs used concurrently: NA. Although Pantecta (pantoprazole, Tablet, Delayed Release) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dyspnoea, may still occur.
Pantecta Side Effect Report#4830692-4
Gastrointestinal Haemorrhage, Haematocrit Decreased, Hiatus Hernia
This Gastrointestinal Haemorrhage problem was reported by a consumer or non-health professional from Spain. A 87-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: duodenitis,gastritis. On
Aug 01, 2003 this consumer started treatment with Pantecta (pantoprazole, Tablet, Delayed Release) (dosage: 40 Mg 1x Per 1 Day, Oral). The following drugs were being taken at the same time: NA. When using Pantecta (pantoprazole, Tablet, Delayed Release), the patient experienced the following unwanted symptoms/side effects: Gastrointestinal Haemorrhage, Haematocrit Decreased, Hiatus HerniaThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Gastrointestinal Haemorrhage, may become evident only after a product is in use by the general population.
Pantecta Side Effect Report#4830610-9
Gastritis
This Gastritis side effect was reported by a health professional from Guatemala. A 71-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Pantecta (pantoprazole, Tablet, Delayed Release) (drug dosage: 40 Mg 1x Per 1 Day Oral), which was initiated on NS. Concurrently used drugs: NA..After starting to take Pantecta (pantoprazole, Tablet, Delayed Release) the consumer reported adverse symptoms, such as: GastritisThese side effects may potentially be related to Pantecta (pantoprazole, Tablet, Delayed Release).
Pantecta Side Effect Report#4745318-8
Endoscopy Upper Gastrointestinal Tract Abnormal, Gastrointestinal Haemorrhage, Hiatus Hernia
This is a report of a 87-year-old male patient (weight: NA) from Spain, suffering from the following health symptoms/conditions: duodenitis,gastritis, who was treated with Pantecta (pantoprazole, Tablet, Delayed Release) (dosage: 40 Mg 1x Per 1 Day, Oral, start time:
Aug 01, 2003), combined with: NA. and developed a serious reaction and side effect(s): Endoscopy Upper Gastrointestinal Tract Abnormal, Gastrointestinal Haemorrhage, Hiatus Hernia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Pantecta (pantoprazole, Tablet, Delayed Release) treatment in male patients, resulting in Endoscopy Upper Gastrointestinal Tract Abnormal side effect. The patient was hospitalized.


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The appearance of Pantecta on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

What are common Pantecta Side Effects for Women?

Women Side Effects Reports
Death 5
Chest Discomfort 3
Fall 3
Osteoporosis 3
Rib Fracture 3
Wheezing 3
Bone Densitometry 2
Dengue Fever 2
Hepatic Failure 2
Renal Failure 2

What are common Pantecta Side Effects for Men?

Men Side Effects Reports
Gastrointestinal Haemorrhage 4
Anaemia 2
Bronchospasm 2
Cardiac Failure 2
Colon Cancer 2
Death 2
Haemorrhage 2
Hiatus Hernia 2
Neutropenia 2
Ulcer 2

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Pantecta reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Pantecta Safety Alerts, Active Ingredients, Usage Information

    More About Pantecta

    Side Effects reported to FDA: 46

    Pantecta safety alerts: No

    Reported deaths: 22

    Reported hospitalizations: 11

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