Common Stillen Side Effects


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

Loss Of Consciousness (2)
Electrolyte Imbalance (1)
Disseminated Tuberculosis (1)
Dehydration (1)
Renal Failure Acute (1)
Gastritis (1)
Hepatic Failure (1)
Oral Candidiasis (1)
Insomnia (1)
Hyperglycaemia (1)
Herpes Simplex (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.

Stillen Side Effects Reported to FDA



Stillen Side Effect Report#8266068-X
Renal Failure Acute, Herpes Simplex, Hyperglycaemia, Electrolyte Imbalance, Oral Candidiasis, Insomnia, Dehydration, Gastritis
This is a report of a 68-year-old male patient (weight: NA) from Korea, Republic Of, suffering from the following health symptoms/conditions: gastritis,hyperglycaemia,antifungal prophylaxis, who was treated with Stillen (dosage: 60 Mg, Daily, start time:
Jun 22, 2010), combined with:
  • Humalog (100 Iu/ml, 10ml, 28 Iu Daily)
  • Ts Tab
  • 3tc/azt (900 Mg, Daily)
  • Amaryl (4 Mg, Daily)
  • Glupa
  • Kaletra
  • Combivir (900 Mg, Daily)
  • C-all
and developed a serious reaction and side effect(s): Renal Failure Acute, Herpes Simplex, Hyperglycaemia, Electrolyte Imbalance, Oral Candidiasis, Insomnia, Dehydration, Gastritis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Stillen treatment in male patients, resulting in Renal Failure Acute side effect. The patient was hospitalized.
Stillen Side Effect Report#8213143-1
Hepatic Failure
This report suggests a potential Stillen Hepatic Failure side effect(s) that can have serious consequences. A 73-year-old female patient (weight: NA) from Korea, Republic Of was diagnosed with the following symptoms/conditions: back pain,upper respiratory tract infection and used Stillen (dosage: Unk) starting
Jan 25, 2012. After starting Stillen the patient began experiencing various side effects, including: Hepatic FailureAdditional drugs used concurrently:
  • Ambroxol (Unk)
  • Codeine Phosphate (Unk)
  • Crizotinib (250 Mg, 2x/day)
  • Ultracet (Unk)
  • Famotidine (Unk)
  • Metoclopramide (Unk)
  • Megestrol Acetate (Unk)
  • Magnesium Oxide (Unk)
The patient was hospitalized. Although Stillen demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hepatic Failure, may still occur.
Stillen Side Effect Report#8138310-7
Loss Of Consciousness
This Loss Of Consciousness problem was reported by a physician from Korea, Republic Of. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: vomiting,nausea,pain management,paraesthesia. On
Dec 29, 2011 this consumer started treatment with Stillen (dosage: NA). The following drugs were being taken at the same time: NA. When using Stillen, the patient experienced the following unwanted symptoms/side effects: Loss Of ConsciousnessAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Loss Of Consciousness, may become evident only after a product is in use by the general population.
Stillen Side Effect Report#8055498-7
Loss Of Consciousness
This Loss Of Consciousness side effect was reported by a physician from Korea, Republic Of. A female patient (weight:NA) experienced the following symptoms/conditions: vomiting,paraesthesia,pain management,nausea.The patient was prescribed Stillen (drug dosage: NA), which was initiated on
Dec 29, 2011. Concurrently used drugs:
  • Opalmon
  • Ultracet
.After starting to take Stillen the consumer reported adverse symptoms, such as: Loss Of ConsciousnessThese side effects may potentially be related to Stillen.
Stillen Side Effect Report#7620130-0
Disseminated Tuberculosis
This is a report of a 36-year-old male patient (weight: NA) from Korea, Republic Of, suffering from the following health symptoms/conditions: NA, who was treated with Stillen (dosage: NA, start time:
May 31, 2007), combined with:
  • Infliximab
  • Infliximab (4th Dose In A Series)
  • Itopride Hcl
  • Corticap
  • Aceclofenac
and developed a serious reaction and side effect(s): Disseminated Tuberculosis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Stillen treatment in male patients, resulting in Disseminated Tuberculosis side effect. The patient was hospitalized.



The appearance of Stillen 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 Stillen Side Effects for Women?

Women Side Effects Reports
Loss Of Consciousness 2
Hepatic Failure 1

What are common Stillen Side Effects for Men?

Men Side Effects Reports
Dehydration 1
Disseminated Tuberculosis 1
Electrolyte Imbalance 1
Gastritis 1
Herpes Simplex 1
Hyperglycaemia 1
Insomnia 1
Oral Candidiasis 1
Renal Failure Acute 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.

    Stillen 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 Stillen

    Side Effects reported to FDA: 5

    Stillen safety alerts: No

    Reported hospitalizations: 4

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