Please choose an event type to view the corresponding MedsFacts report:

INSOMNIA ( 32 FDA reports)
HEADACHE ( 26 FDA reports)
NASOPHARYNGITIS ( 26 FDA reports)
SINUS HEADACHE ( 16 FDA reports)
DIZZINESS ( 15 FDA reports)
DYSPNOEA ( 13 FDA reports)
HEART RATE INCREASED ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
ANOREXIA ( 12 FDA reports)
CHEST PAIN ( 12 FDA reports)
UNEVALUABLE EVENT ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
SINUS CONGESTION ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
VOMITING ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
FEELING JITTERY ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
INITIAL INSOMNIA ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
RASH ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FALL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TENSION ( 1 FDA reports)
THIRST ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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