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

DRUG INEFFECTIVE ( 400 FDA reports)
NASAL CONGESTION ( 51 FDA reports)
HEADACHE ( 39 FDA reports)
DYSPNOEA ( 37 FDA reports)
DRUG EFFECT DECREASED ( 21 FDA reports)
SOMNOLENCE ( 20 FDA reports)
INSOMNIA ( 18 FDA reports)
URTICARIA ( 18 FDA reports)
DIZZINESS ( 17 FDA reports)
SINUS HEADACHE ( 17 FDA reports)
MALAISE ( 16 FDA reports)
RHINORRHOEA ( 15 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
FATIGUE ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
SNEEZING ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
COLD SWEAT ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NASAL OEDEMA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
COUGH ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
APATHY ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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