Common Tanezumab Side Effects


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

Gastritis (1)
Duodenal Ulcer (1)
Gastrointestinal Haemorrhage (1)
Joint Stiffness (1)
Anaemia (1)
Condition Aggravated (1)
Cardiac Arrest (1)
Oedema Peripheral (1)
Arthralgia (1)
Paraesthesia (1)
Tremor (1)
Arthritis (1)
Musculoskeletal Pain (1)


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.

Tanezumab Side Effects Reported to FDA


Tanezumab Side Effect Report#8204406-4
Condition Aggravated, Arthritis
This is a report of a 59-year-old male patient (weight: NA) from United States, suffering from the following health symptoms/conditions: arthritis, who was treated with Tanezumab (dosage: 1 0z, start time:
Jun 01, 2008), combined with: NA. and developed a serious reaction and side effect(s): Condition Aggravated, Arthritis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Tanezumab treatment in male patients, resulting in Condition Aggravated side effect.
Tanezumab Side Effect Report#7911959-X
Cardiac Arrest
This report suggests a potential Tanezumab (tanezumab) Cardiac Arrest side effect(s) that can have serious consequences. A 78-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: back pain and used Tanezumab (tanezumab) (dosage: (20 Mg), Intravenous) starting
Jan 01, 2006. After starting Tanezumab (tanezumab) the patient began experiencing various side effects, including: Cardiac ArrestAdditional drugs used concurrently:
  • Prilosec
  • Metoprolol Tartrate (Oral)
The patient was hospitalized. Although Tanezumab (tanezumab) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Cardiac Arrest, may still occur.
Tanezumab Side Effect Report#7284470-X
Gastritis, Duodenal Ulcer, Gastrointestinal Haemorrhage, Anaemia
This Gastritis problem was reported by a physician from United States. A 71-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: osteoarthritis,hypertension. On
Jan 10, 2009 this consumer started treatment with Tanezumab (dosage: Q 8 Weeks). The following drugs were being taken at the same time:
  • Prinivil (10 - 12.5mg)
  • Mobic (7.5 Mg)
  • Celexa (40 Mg)
  • Aspirin (81 Mg)
  • Ultram (50 Mg)
  • Magnesium (500mg As Needed)
  • Prilosec (40 Mg)
When using Tanezumab, the patient experienced the following unwanted symptoms/side effects: Gastritis, Duodenal Ulcer, Gastrointestinal Haemorrhage, AnaemiaThe 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 Gastritis, may become evident only after a product is in use by the general population.
Tanezumab Side Effect Report#7250589-2
Tremor, Joint Stiffness, Musculoskeletal Pain, Arthralgia, Oedema Peripheral, Paraesthesia
This Tremor side effect was reported by a consumer or non-health professional from United States. A 50-year-old female patient (weight:NA) experienced the following symptoms/conditions: arthritis.The patient was prescribed Tanezumab Pfizer (drug dosage: Every 2 Months), which was initiated on
Mar 10, 2009. Concurrently used drugs: NA..After starting to take Tanezumab Pfizer the consumer reported adverse symptoms, such as: Tremor, Joint Stiffness, Musculoskeletal Pain, Arthralgia, Oedema Peripheral, ParaesthesiaThese side effects may potentially be related to Tanezumab Pfizer.



The appearance of Tanezumab 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 Tanezumab Side Effects for Women?

Women Side Effects Reports
Anaemia 1
Arthralgia 1
Cardiac Arrest 1
Duodenal Ulcer 1
Gastritis 1
Gastrointestinal Haemorrhage 1
Joint Stiffness 1
Musculoskeletal Pain 1
Oedema Peripheral 1
Paraesthesia 1

What are common Tanezumab Side Effects for Men?

Men Side Effects Reports
Arthritis 1
Condition Aggravated 1

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.

    Tanezumab 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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    More About Tanezumab

    Side Effects reported to FDA: 4

    Tanezumab safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 1

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