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Herbessor Side Effects

Common Herbessor Side Effects


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

Trousseau's Syndrome (2)
Cerebral Infarction (2)
Pyrexia (1)
Pneumonia Bacterial (1)
Renal Tubular Necrosis (1)
Oxygen Saturation Decreased (1)
Malignant Neoplasm Progression (1)
Inappropriate Antidiuretic Hormone Secretion (1)
Kidney Transplant Rejection (1)
Malaise (1)
Dyspnoea (1)
Cholecystitis Acute (1)
Abdominal Pain (1)
C-reactive Protein Increased (1)
Cardio-respiratory Arrest (1)
Respiratory Failure (1)
Blood Sodium Decreased (1)
Blood Potassium Decreased (1)
Blood Pressure Decreased (1)
Depressed Level Of Consciousness (1)

➢ 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.

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.

Herbessor Side Effects Reported to FDA

The following Herbessor 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.


The appearance of Herbessor 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.
Malaise, Oxygen Saturation Decreased, Blood Pressure Decreased, Respiratory Failure, Cardio-respiratory Arrest, Depressed Level Of Consciousness, Pneumonia Bacterial, Dyspnoea, C-reactive Protein Increased
This is a report of a male patient (weight: NA) from JAPAN, suffering from the following symptoms/conditions: NA, who was treated with Herbessor (dosage: 200 Mg, Unk, start time: Jul 12, 2010), combined with:
  • Femara (2.5 Mg, Daily)
  • Procylin (60 Ug, Unk)
  • Actos (15 Mg, Unk)
  • Lanirapid (0.05 Mg, Unk)
  • Aspirin (100 Mg, Unk)
  • Isosorbide Dinitrate (40 Mg, Unk)
  • Famotidine (40 Mg, Unk)
  • Sucralfate (3 G, Unk)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Malaise
  • Oxygen Saturation Decreased
  • Blood Pressure Decreased
  • Respiratory Failure
  • Cardio-respiratory Arrest
  • Depressed Level Of Consciousness
  • Pneumonia Bacterial
  • Dyspnoea
  • C-reactive Protein Increased
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Herbessor treatment in male patients, resulting in malaise side effect. The patient was hospitalized.

Renal Tubular Necrosis, Kidney Transplant Rejection, Cholecystitis Acute, Pyrexia, Abdominal Pain
This report suggests a potential Herbessor R Renal Tubular Necrosis, Kidney Transplant Rejection, Cholecystitis Acute, Pyrexia, Abdominal Pain side effect(s) that can have serious consequences. A male patient (weight: NA) from JAPAN was diagnosed with the following symptoms/conditions: ischaemic heart disease prophylaxis and used Herbessor R (dosage: 100 Mg,) starting Jan 28, 2005. Soon after starting Herbessor R the patient began experiencing various side effects, including:
  • Renal Tubular Necrosis
  • Kidney Transplant Rejection
  • Cholecystitis Acute
  • Pyrexia
  • Abdominal Pain
Drugs used concurrently:
  • Sigmart (15 Mg,)
  • Cellcept
  • Solu-medrol (500 Mg,)
  • Simulect (20 Mg,)
  • Rabeprazole Sodium (1 Df,)
  • Prednisolone
  • Neoral
  • Simulect (20 Mg,)
Although Herbessor R demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as renal tubular necrosis, may still occur.

Blood Potassium Decreased
This Blood Potassium Decreased problem was reported by a pharmacist from JAPAN. A 81-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On Jun 03, 2010 this consumer started treatment with Herbessor R (dosage: 100 Mg, Unk). The following drugs were being taken at the same time:
  • Evista (60 Mg, Unk)
  • Neurotropin (2 Df, Unk)
  • Onealfa (1 Mg, Qd)
  • Diovan (80 Mg, Qd)
  • Aricept (10 Mg, Unk)
When commencing Herbessor R, the patient experienced the following unwanted symptoms/side effects:
  • Blood Potassium Decreased
Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as blood potassium decreased, may become evident only after a product is in use by the general population.

Cerebral Infarction, Malignant Neoplasm Progression, Trousseau's Syndrome
This is a report of a 60-year-old female patient (weight: NA) from JAPAN. The patient developed the following symptoms/conditions: angina pectoris and was treated with Herbessor R (dosage: 1 D/f, Daily (1/d)) starting Jul 04, 2005. Concurrently used drugs:
  • Aspirin (1 D/f, Daily (1/d))
  • Pariet /jpn/ (1 D/f, Daily (1/d))
  • Aspara-ca (2 D/f, Daily (1/d))
  • Glakay (3 D/f, Daily (1/d))
  • One-alpha (2 D/f, Daily (1/d))
  • Gemzar (1600 Mg, Other)
  • Gemzar (1600 Mg, Other)
Soon after that, the consumer experienced the following side effects:
  • Cerebral Infarction
  • Malignant Neoplasm Progression
  • Trousseau's Syndrome
The patient was hospitalized. This opens a possibility that Herbessor R treatment could cause the above reactions, including cerebral infarction, and some female subjects may be more susceptible.


Cerebral Infarction, Trousseau's Syndrome
A 60-year-old female patient (weight: NA) from JAPAN with the following symptoms/conditions: angina pectoris started Herbessor R treatment (dosage: 1 D/f, Daily (1/d)) on Jul 04, 2005. Soon after starting Herbessor R treatment, the subject experienced various side effects, including:
  • Cerebral Infarction
  • Trousseau's Syndrome
Concurrently used drugs:
  • Aspirin (1 D/f, Daily (1/d))
  • Pariet /jpn/ (1 D/f, Daily (1/d))
  • Aspara-ca (2 D/f, Daily (1/d))
  • Glakay (3 D/f, Daily (1/d))
  • One-alpha (2 D/f, Daily (1/d))
  • Gemzar (1600 Mg, Other)
  • Gemzar (1600 Mg, Other)
The patient was hospitalized. This finding indicates that some female patients could be more vulnerable to Herbessor R.

Antinuclear Antibody Increased, Blood Sodium Decreased, Inappropriate Antidiuretic Hormone Secretion
A 78-year-old male patient from JAPAN (weight: NA) experienced symptoms, such as: NA and was treated with Herbessor R(dosage: 1 Df, Unk). The treatment was initiated on NS. After that a consumer reported the following side effect(s):
  • Antinuclear Antibody Increased
  • Blood Sodium Decreased
  • Inappropriate Antidiuretic Hormone Secretion
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Herbessor R efficacy:
  • Tamsulosin Hydrochloride (0.2 Mg, Unk)
  • Flivas (25 Mg, Unk)
  • Sennoside (4 Df, Unk)
  • Magnesium Oxide (1 Df, Unk)
  • Cyanocobalamin (1 Df, Unk)
  • Eviprostat (0.2 Mg, Unk)
  • Warfarin Sodium (25 Mg, Unk)
  • Cerocral (1 Df, Unk)
The patient was hospitalized.



Keep Track of Side Effects

Note Your Observations

It is really important to keep of your 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

    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.


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    More About Herbessor

    Side Effects reported to FDA: 6

    Herbessor safety alerts: No

    Reported deaths: 2

    Reported hospitalizations: 3

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