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BLOOD GLUCOSE INCREASED ( 372 FDA reports)
NAUSEA ( 201 FDA reports)
WEIGHT DECREASED ( 163 FDA reports)
BLOOD GLUCOSE DECREASED ( 136 FDA reports)
DECREASED APPETITE ( 98 FDA reports)
INCORRECT DOSE ADMINISTERED ( 65 FDA reports)
DIZZINESS ( 52 FDA reports)
VOMITING ( 51 FDA reports)
DRUG EFFECT DECREASED ( 49 FDA reports)
TREMOR ( 48 FDA reports)
DRUG INEFFECTIVE ( 47 FDA reports)
INJECTION SITE PAIN ( 38 FDA reports)
FATIGUE ( 37 FDA reports)
DIARRHOEA ( 34 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 34 FDA reports)
FEELING ABNORMAL ( 33 FDA reports)
HEADACHE ( 32 FDA reports)
WEIGHT INCREASED ( 31 FDA reports)
INJECTION SITE BRUISING ( 30 FDA reports)
INJECTION SITE HAEMORRHAGE ( 26 FDA reports)
ASTHENIA ( 24 FDA reports)
HYPERHIDROSIS ( 23 FDA reports)
MALAISE ( 23 FDA reports)
ABDOMINAL PAIN UPPER ( 20 FDA reports)
SOMNOLENCE ( 18 FDA reports)
ABDOMINAL DISTENSION ( 17 FDA reports)
CONSTIPATION ( 15 FDA reports)
DYSPEPSIA ( 15 FDA reports)
FEELING JITTERY ( 15 FDA reports)
EARLY SATIETY ( 14 FDA reports)
VISION BLURRED ( 14 FDA reports)
ANOREXIA ( 12 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 12 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 12 FDA reports)
HUNGER ( 12 FDA reports)
ACCIDENTAL OVERDOSE ( 11 FDA reports)
ERUCTATION ( 11 FDA reports)
INJECTION SITE EXTRAVASATION ( 11 FDA reports)
IRRITABILITY ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
CHILLS ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
FEELING COLD ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
DYSGEUSIA ( 9 FDA reports)
FLATULENCE ( 9 FDA reports)
INJECTION SITE HAEMATOMA ( 9 FDA reports)
INJECTION SITE IRRITATION ( 9 FDA reports)
NASOPHARYNGITIS ( 9 FDA reports)
CHEST PAIN ( 8 FDA reports)
COUGH ( 8 FDA reports)
PAIN ( 8 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 7 FDA reports)
INCREASED APPETITE ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
RETCHING ( 7 FDA reports)
STRESS ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
BACK PAIN ( 5 FDA reports)
FALL ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
NASAL CONGESTION ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INJECTION SITE URTICARIA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
RASH ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CATARACT ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
THIRST ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE LACERATION ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SWELLING ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGER ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD GLUCAGON DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENOPAUSE DELAYED ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)

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