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Hypromellose Side Effects

Common Hypromellose Side Effects


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

Pain (2)
Hypophagia (1)
Vomiting (1)
Visual Acuity Reduced (1)
Headache (1)
Haematemesis (1)
Asthenia (1)
Anxiety (1)
Abdominal Pain Lower (1)
Vision Blurred (1)
Syncope (1)
Malaise (1)
Loss Of Consciousness (1)
Infection (1)
Muscle Rigidity (1)
Pathological Fracture (1)
Sedation (1)
Respiratory Rate Increased (1)
Product Deposit (1)
Tremor (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.

Hypromellose Side Effects Reported to FDA

The following Hypromellose 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 Hypromellose 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.
Convulsion, Respiratory Rate Increased, Muscle Rigidity, Loss Of Consciousness, Tremor
This is a report of a 85-year-old female patient (weight: NA) from GB, suffering from the following symptoms/conditions: NA, who was treated with Hypromellose (dosage: NA, start time: Feb 22, 2013), combined with:
  • Simvastatin (At Night.)
  • Xalacom
  • Atenolol
  • Amlodipine
  • Lactulose (As Necessary)
  • Donepezil (At Night. 4 Doses.)
  • Senna (At Night.)
  • Hydrochlorothiazide W/irbesartan (150//12.5mg)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Convulsion
  • Respiratory Rate Increased
  • Muscle Rigidity
  • Loss Of Consciousness
  • Tremor
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Hypromellose treatment in female patients, resulting in convulsion side effect.

Dacryostenosis Acquired, Chalazion, Eye Infection
This report suggests a potential Hypromelloses Dacryostenosis Acquired, Chalazion, Eye Infection side effect(s) that can have serious consequences. A 30-year-old female patient (weight: NA) from US was diagnosed with the following symptoms/conditions: dry eye,gastrooesophageal reflux disease,polycystic ovaries,hypertension and used Hypromelloses (dosage: Unk Ukn, Unk) starting NS. Soon after starting Hypromelloses the patient began experiencing various side effects, including:
  • Dacryostenosis Acquired
  • Chalazion
  • Eye Infection
Drugs used concurrently:
  • Nexium
  • Spironolactone (50 Mg, Bid)
  • Lisinopril (10 Mg, Qd)
  • Sprintec
  • Restasis (Unk Ukn, Bid)
  • Xyzal (5 Mg, Qd)
  • Neurontin (300 Mg, Bid)
  • Flexeril
Although Hypromelloses demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as dacryostenosis acquired, may still occur.

Pain
This Pain problem was reported by a health professional from . A 72-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On Oct 27, 2011 this consumer started treatment with Hypromellose (hypromellose) (dosage: NA). The following drugs were being taken at the same time:
  • Alendronic Acid (alendronic Acid)
  • Prednisolone
  • Valsartan
  • Ventolin
  • Belometasone (beclometasone)
  • Lansoprazole
  • Doxycycline
  • Simvastatin
When commencing Hypromellose (hypromellose), the patient experienced the following unwanted symptoms/side effects:
  • Pain
Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as pain, may become evident only after a product is in use by the general population.

Pain
This is a report of a 72-year-old female patient (weight: NA) from UNITED KINGDOM. The patient developed the following symptoms/conditions: NA and was treated with Hypromellose (dosage: NA) starting Nov 07, 2011. Concurrently used drugs:
  • Prednisolone
  • Beclomethasone Dipropionate
  • Zocor
  • Folic Acid
  • Lansoprazole
  • Diclofenac Sodium
  • Alendronate Sodium
  • Bendroflumethiazide
Soon after that, the consumer experienced the following side effects:
  • Pain
This opens a possibility that Hypromellose treatment could cause the above reactions, including pain, and some female subjects may be more susceptible.


Product Deposit, Visual Acuity Reduced
A 80-year-old female patient (weight: NA) from SWEDEN with the following symptoms/conditions: NA started Hypromellose treatment (dosage: NA) on Dec 29, 2011. Soon after starting Hypromellose treatment, the subject experienced various side effects, including:
  • Product Deposit
  • Visual Acuity Reduced
Concurrently used drugs:
  • Trusopt
  • Fusidic Acid
  • Bimatoprost
This finding indicates that some female patients could be more vulnerable to Hypromellose.

Sedation, Vision Blurred, Headache, Anxiety, Dizziness
A 74-year-old female patient from UNITED KINGDOM (weight: NA) experienced symptoms, such as: NA and was treated with Hypromellose(dosage: NA). The treatment was initiated on Mar 08, 2011. After that a consumer reported the following side effect(s):
  • Sedation
  • Vision Blurred
  • Headache
  • Anxiety
  • Dizziness
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Hypromellose efficacy: NA.

Infection, Syncope, Vomiting
In this report, Hypromellose was administered for the following condition: NA.A 74-year-old female consumer from UNITED KINGDOM (weight: NA) started Hypromellose treatment (dosage: NA) on Nov 24, 2010.Sometime after starting the treatment, the patient complained of the following side effect(s):
  • Infection
  • Syncope
  • Vomiting
A possible interaction with other drugs could have contributed to this reaction:
  • Golimumab
  • Metformin Hcl
  • Methotrexate (9 Times 2.5mg)
  • Golimumab
  • Acetaminophen And Codeine Phosphate (30/500, As Necessary)
  • Levothyroxine
  • Folic Acid
  • Adcal D3
The patient was hospitalized.Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Hypromellose treatment could be related to the listed above side effect(s).

Haematemesis
This is a report of the following Hypromellose side effect(s):
  • Haematemesis
A 75-year-old female patient from UNITED KINGDOM (weight: NA) presented with the following condition: NA and received a treatment with Hypromellose (dosage: NA) starting: NS.The following concurrently used drugs could have generated interactions:
  • Furosemide
  • Ibuprofen
  • Simvastatin
  • Naproxen Sodium
  • Quinine Sulfate
  • Sodium Bicarbonate
  • Acetylsalicylic Acid Srt (75 Mg, Qd)
  • Algesal [diethylamine Salicylate]
The patient was hospitalized.This report suggests that a Hypromellose treatment could be associated with the listed above side effect(s).

Pathological Fracture
This Hypromellose report was submitted by a 80-year-old female consumer from SWEDEN (weight: NA). The patient was diagnosed with: NA and Hypromellose was administered (dosage: NA) starting: Mar 01, 2007. The consumer developed a set of symptoms:
  • Pathological Fracture
Other drugs used simultaneously:
  • Paroxetine
  • Fosamax
  • Strontium Ranelate
  • Acetaminophen
  • Estriol
  • Calcium Carbonate And Cholecalciferol
  • Omeprazole
  • Simethicone
The patient was hospitalized.Those unexpected symptoms could be linked to a Hypromellose treatment, however establishing a potential drug-safety problem requires a more detailed clinical analysis.

Blood Pressure Increased
This is a report of a possible correlation between Hypromellose use and the following symptoms/side effect(s):
  • Blood Pressure Increased
which could contribute to an assessment of Hypromellose risk profile.A 63-year-old female consumer from UNITED KINGDOM (weight: NA) was suffering from NA and was treated with Hypromellose (dosage: NA) starting Dec 01, 2010.Other concurrent medications:
  • Mometasone Furoate (Nas)
  • Dothiepin Hydrochloride
  • Naratriptan
  • Rosuvastatin
  • Meloxicam
  • Hydrochloride
  • Perindopril Erbumine


Hypophagia, Weight Decreased, Malaise, Clostridial Infection, Cyanosis, Abdominal Pain Lower, Asthenia, Blood Pressure Decreased
A 88-year-old female patient from UNITED KINGDOM (weight: NA) presented with the following symptoms: NA and after a treatment with Hypromellose (dosage: NA) experienced the following side effect(s):
  • Hypophagia
  • Weight Decreased
  • Malaise
  • Clostridial Infection
  • Cyanosis
  • Abdominal Pain Lower
  • Asthenia
  • Blood Pressure Decreased
The treatment was started on Oct 09, 2009. Hypromellose was used in combination with the following drugs:
  • Simvastatin
  • Amoxicillin (1gm 12 Doses Iv)
  • Enoxaparin
  • Metronidazole (500 Mg 2 Doses Iv)
  • Piperacillin Sodium As Tazocin (4.5g 1 Dose Iv)
  • Nicorandil
  • Paracetamol
  • Tazobactam Sodium As Tazocin (4.5g 3 Doses Iv)
The patient was hospitalized.This report could alert potential Hypromellose consumers.

Extrasystoles
In this report, a 78-year-old female patient from UNITED KINGDOM (weight: NA) was affected by a possible Hypromellose side effect.The patient was diagnosed with NA. After a treatment with Hypromellose (dosage: Unk, start date: Mar 15, 2007), the patient experienced the following side effect(s):
  • Extrasystoles
The following simultaneously used drugs could have led to this reaction:
  • Plavix
  • Plavix
The findings here stress that side effects should be taken into consideration when evaluating a Hypromellose treatment.



Top 10 Hypromellose Side Effects for Women

Women Side EffectsReports
Pain 2
Abdominal Pain Lower 1
Anxiety 1
Asthenia 1
Blood Pressure Decreased 1
Blood Pressure Increased 1
Chalazion 1
Clostridial Infection 1
Convulsion 1
Cyanosis 1

Top 10 Hypromellose Side Effects for Men

Men Side EffectsReports

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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    Hypromellose Safety Alerts, Active Ingredients, Usage Information

    NDC17478-064
    TypeHUMAN PRESCRIPTION DRUG
    Proprietary NameGonak Hypromellose
    NameHypromellose 2906 (4000 MPA.S) and Hypromellose 2906 (50 MPA.S)
    Dosage FormSOLUTION
    RouteOPHTHALMIC
    On market since19970101
    LabelerAkorn, Inc.
    Active Ingredient(s)HYPROMELLOSE 2906 (4000 MPA.S); HYPROMELLOSE 2906 (50 MPA.S)
    Strength(s)25; 25
    Unit(s)mg/mL; mg/mL
    Pharma Class

    More About Hypromellose

    Side Effects reported to FDA: 12

    Hypromellose safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 4

    Latest Hypromellose clinical trials