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

SINUSITIS ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
PAIN ( 4 FDA reports)
VOMITING ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
CRYING ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
MALAISE ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
ABASIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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