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YELLOW SKIN ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
CONVULSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLIATIVE CARE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
ACNE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)

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